Linked Data
ClinVar Variation Id:
14270
ClinVar RCV Id:
RCV000015340
dbSNP Id:
rs1553701477
PubMed:
PMID:7874167
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.69936756G>A , CM000665.2:g.69936756G>A | GRCh38 |
| NC_000003.11:g.69985907G>A , CM000665.1:g.69985907G>A | GRCh37 |
| NC_000003.10:g.70068597G>A | NCBI36 |
| NG_011631.1:g.202275G>A , LRG_776:g.202275G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000314589.11:c.307-1066G>A | ENSP00000324443.5:n.307-1066G>A | |
| ENST00000687384.1:c.304-1066G>A | ENSP00000510225.1:n.304-1066G>A | |
| ENST00000689390.1:n.529-1066G>A | ||
| ENST00000693031.1:c.355-1066G>A | ENSP00000509845.1:n.355-1066G>A | |
| ENST00000693549.1:c.307-1066G>A | ENSP00000509358.1:n.307-1066G>A | |
| ENST00000314589.10:c.307-1066G>A | ENSP00000324443.5:n.307-1066G>A | |
| ENST00000352241.9:c.355-1066G>A MANE Select | ENSP00000295600.8:n.355-1066G>A | |
| ENST00000394351.9:c.33+1G>A MANE Plus Clinical | ENSP00000377880.3:n.33+1G>A | |
| ENST00000448226.9:c.352-1066G>A | ENSP00000391803.3:n.352-1066G>A | |
| ENST00000642352.1:c.355-1066G>A | ENSP00000494105.1:n.355-1066G>A | |
| ENST00000314557.10:c.33+1G>A | ENSP00000324246.6:n.33+1G>A | |
| ENST00000314589.9:c.307-1066G>A | ENSP00000324443.5:n.307-1066G>A | |
| ENST00000328528.10:c.352-1066G>A | ENSP00000327867.6:n.352-1066G>A | |
| ENST00000352241.8:c.355-1066G>A | ENSP00000295600.7:n.355-1066G>A | |
| ENST00000394348.2:c.33+1G>A | ENSP00000481286.1:n.33+1G>A | |
| ENST00000394351.7:c.33+1G>A | ENSP00000377880.3:n.33+1G>A | |
| ENST00000429090.5:c.199-1066G>A | ENSP00000407620.1:n.199-1066G>A | |
| ENST00000433517.5:c.199-1066G>A | ENSP00000411389.1:n.199-1066G>A | |
| ENST00000448226.6:c.355-1066G>A | ENSP00000391803.2:n.355-1066G>A | |
| ENST00000451708.5:c.307-1066G>A | ENSP00000398639.1:n.307-1066G>A | |
| ENST00000472437.5:c.199-1066G>A | ENSP00000418845.1:n.199-1066G>A | |
| ENST00000478490.5:c.33+1G>A | ENSP00000433487.1:n.33+1G>A | |
| ENST00000531774.1:c.33+1G>A | ENSP00000435909.1:n.33+1G>A | |
| NM_000248.3:c.33+1G>A , LRG_776t1:c.33+1G>A | NP_000239.1:n.33+1G>A | |
| NM_001184967.1:c.199-1066G>A | NP_001171896.1:n.199-1066G>A | |
| NM_001184968.1:c.33+1G>A | NP_001171897.1:n.33+1G>A | |
| NM_006722.2:c.352-1066G>A | NP_006713.1:n.352-1066G>A | |
| NM_198158.2:c.33+1G>A | NP_937801.1:n.33+1G>A | |
| NM_198159.2:c.355-1066G>A | NP_937802.1:n.355-1066G>A | |
| NM_198177.2:c.307-1066G>A | NP_937820.1:n.307-1066G>A | |
| NM_198178.2:c.33+1G>A | NP_937821.2:n.33+1G>A | |
| XM_005264754.1:c.355-1066G>A | XP_005264811.1:n.355-1066G>A | |
| XM_005264755.2:c.307-1066G>A | XP_005264812.1:n.307-1066G>A | |
| XM_006713164.2:c.199-1066G>A | XP_006713227.1:n.199-1066G>A | |
| XM_011533722.1:c.352-1066G>A | XP_011532024.1:n.352-1066G>A | |
| XM_011533723.1:c.304-1066G>A | XP_011532025.1:n.304-1066G>A | |
| XM_011533724.1:c.199-1066G>A | XP_011532026.1:n.199-1066G>A | |
| XM_011533725.1:c.355-1066G>A | XP_011532027.1:n.355-1066G>A | |
| XM_011533726.1:c.355-1066G>A | XP_011532028.1:n.355-1066G>A | |
| NM_001354604.1:c.355-1066G>A | NP_001341533.1:n.355-1066G>A | |
| NM_001354605.1:c.352-1066G>A | NP_001341534.1:n.352-1066G>A | |
| NM_001354606.1:c.352-1066G>A | NP_001341535.1:n.352-1066G>A | |
| NM_001354607.1:c.304-1066G>A | NP_001341536.1:n.304-1066G>A | |
| NM_001354608.1:c.199-1066G>A | NP_001341537.1:n.199-1066G>A | |
| NM_001184967.2:c.199-1066G>A | NP_001171896.1:n.199-1066G>A | |
| NM_001184968.2:c.33+1G>A | NP_001171897.1:n.33+1G>A | |
| NM_001354604.2:c.355-1066G>A MANE Select | NP_001341533.1:n.355-1066G>A | |
| NM_001354605.2:c.352-1066G>A | NP_001341534.1:n.352-1066G>A | |
| NM_001354606.2:c.352-1066G>A | NP_001341535.1:n.352-1066G>A | |
| NM_001354607.2:c.304-1066G>A | NP_001341536.1:n.304-1066G>A | |
| NM_001354608.2:c.199-1066G>A | NP_001341537.1:n.199-1066G>A | |
| NM_198158.3:c.33+1G>A | NP_937801.1:n.33+1G>A | |
| NM_198159.3:c.355-1066G>A | NP_937802.1:n.355-1066G>A | |
| NM_198177.3:c.307-1066G>A | NP_937820.1:n.307-1066G>A | |
| NM_198178.3:c.33+1G>A | NP_937821.2:n.33+1G>A | |
| NM_000248.4:c.33+1G>A MANE Plus Clinical | NP_000239.1:n.33+1G>A | |
| NM_006722.3:c.352-1066G>A | NP_006713.1:n.352-1066G>A |