Linked Data
dbSNP Id:
rs1257542607
gnomAD v2:
2-44184386-C-A
gnomAD v3:
2-43957247-C-A
gnomAD v4:
2-43957247-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43957247C>A , CM000664.2:g.43957247C>A | GRCh38 |
| NC_000002.11:g.44184386C>A , CM000664.1:g.44184386C>A | GRCh37 |
| NC_000002.10:g.44037890C>A | NCBI36 |
| NG_008247.1:g.43759G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409659.6:c.1649+138G>T | ENSP00000386562.2:n.1649+138G>T | |
| ENST00000447246.2:c.1649+138G>T | ENSP00000403637.2:n.1649+138G>T | |
| ENST00000467058.2:n.378+138G>T | ||
| ENST00000681959.1:n.1263+138G>T | ||
| ENST00000681961.1:n.1669+138G>T | ||
| ENST00000682104.1:c.1523+138G>T | ENSP00000507716.1:n.1523+138G>T | |
| ENST00000682303.1:c.*1521+138G>T | ENSP00000508325.1:n.*1521+138G>T | |
| ENST00000682308.1:c.1649+138G>T | ENSP00000507056.1:n.1649+138G>T | |
| ENST00000682480.1:c.1649+138G>T | ENSP00000508344.1:n.1649+138G>T | |
| ENST00000682546.1:c.1649+138G>T | ENSP00000508188.1:n.1649+138G>T | |
| ENST00000682585.1:c.1649+138G>T | ENSP00000506885.1:n.1649+138G>T | |
| ENST00000682595.1:n.2231+138G>T | ||
| ENST00000682607.1:c.67+138G>T | ||
| ENST00000682779.1:c.1640+138G>T | ENSP00000507947.1:n.1640+138G>T | |
| ENST00000682885.1:c.1649+138G>T | ENSP00000508036.1:n.1649+138G>T | |
| ENST00000682933.1:n.1723+138G>T | ||
| ENST00000683072.1:n.2231+138G>T | ||
| ENST00000683082.1:n.1667+138G>T | ||
| ENST00000683125.1:c.1649+138G>T | ENSP00000507939.1:n.1649+138G>T | |
| ENST00000683213.1:c.1652+138G>T | ENSP00000507751.1:n.1652+138G>T | |
| ENST00000683220.1:c.1649+138G>T | ENSP00000507151.1:n.1649+138G>T | |
| ENST00000683329.1:n.2452+138G>T | ||
| ENST00000683346.1:c.*1524+138G>T | ENSP00000507458.1:n.*1524+138G>T | |
| ENST00000683459.1:n.2236+138G>T | ||
| ENST00000683590.1:c.1649+138G>T | ENSP00000506820.1:n.1649+138G>T | |
| ENST00000683623.1:c.1649+138G>T | ENSP00000507702.1:n.1649+138G>T | |
| ENST00000683645.1:n.2169+138G>T | ||
| ENST00000683694.1:n.400+138G>T | ||
| ENST00000683796.1:c.*1521+138G>T | ENSP00000508221.1:n.*1521+138G>T | |
| ENST00000683802.1:n.4574+138G>T | ||
| ENST00000683833.1:c.1640+138G>T | ENSP00000506852.1:n.1640+138G>T | |
| ENST00000683934.1:c.1535+138G>T | ||
| ENST00000683989.1:c.1649+138G>T | ENSP00000507510.1:n.1649+138G>T | |
| ENST00000683994.1:c.1649+138G>T | ENSP00000507181.1:n.1649+138G>T | |
| ENST00000684290.1:c.1649+138G>T | ENSP00000507243.1:n.1649+138G>T | |
| ENST00000684306.1:c.*1562+138G>T | ENSP00000508384.1:n.*1562+138G>T | |
| ENST00000684341.1:n.1669+138G>T | ||
| ENST00000684383.1:c.*1287+138G>T | ENSP00000506863.1:n.*1287+138G>T | |
| ENST00000684482.1:c.4118+138G>T | ||
| ENST00000684619.1:c.*1521+138G>T | ENSP00000508088.1:n.*1521+138G>T | |
| ENST00000684743.1:n.2680+138G>T | ||
| ENST00000260665.12:c.1649+138G>T MANE Select | ENSP00000260665.7:n.1649+138G>T | |
| ENST00000260665.11:c.1649+138G>T | ENSP00000260665.7:n.1649+138G>T | |
| ENST00000467058.1:n.378+138G>T | ||
| NM_133259.3:c.1649+138G>T | NP_573566.2:n.1649+138G>T | |
| XM_006711915.2:c.1571+138G>T | XP_006711978.1:n.1571+138G>T | |
| XM_006711916.2:c.1649+138G>T | XP_006711979.1:n.1649+138G>T | |
| XM_011532473.1:c.1649+138G>T | XP_011530775.1:n.1649+138G>T | |
| XM_011532474.1:c.1649+138G>T | XP_011530776.1:n.1649+138G>T | |
| XM_006711916.3:c.1649+138G>T | XP_006711979.1:n.1649+138G>T | |
| XM_017003117.1:c.1571+138G>T | XP_016858606.1:n.1571+138G>T | |
| XR_002958896.1:n.1691+138G>T | ||
| NM_133259.4:c.1649+138G>T MANE Select | NP_573566.2:n.1649+138G>T |