Linked Data
ClinVar Variation Id:
1574929
ClinVar RCV Id:
RCV002083185
dbSNP Id:
rs777302843
ExAC:
2:203421033 G / A
gnomAD v2:
2-203421033-G-A
gnomAD v4:
2-202556310-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202556310G>A , CM000664.2:g.202556310G>A | GRCh38 |
| NC_000002.11:g.203421033G>A , CM000664.1:g.203421033G>A | GRCh37 |
| NC_000002.10:g.203129278G>A | NCBI36 |
| NG_009363.1:g.184984G>A , LRG_712:g.184984G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.2645G>A MANE Select | ENSP00000363708.4:p.Gly882Asp | |
| ENST00000638587.1:c.2576G>A | ENSP00000491062.1:n.2576G>A | |
| ENST00000374574.2:c.1587-3386G>A | ENSP00000363702.2:n.1587-3386G>A | |
| ENST00000374580.8:c.2645G>A | ENSP00000363708.4:p.Gly882Asp | |
| NM_001204.6:c.2645G>A , LRG_712t1:c.2645G>A | NP_001195.2:p.Gly882Asp | |
| XM_011511687.1:c.2645G>A | XP_011509989.1:p.Gly882Asp | |
| XM_011511688.1:c.1587-3386G>A | XP_011509990.1:n.1587-3386G>A | |
| NM_001204.7:c.2645G>A MANE Select | NP_001195.2:p.Gly882Asp |