Linked Data
ClinVar Variation Id:
307556
dbSNP Id:
rs116845100
ExAC:
12:124172721 G / A
gnomAD v2:
12-124172721-G-A
gnomAD v3:
12-123688174-G-A
gnomAD v4:
12-123688174-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.123688174G>A , CM000674.2:g.123688174G>A | GRCh38 |
| NC_000012.11:g.124172721G>A , CM000674.1:g.124172721G>A | GRCh37 |
| NC_000012.10:g.122738674G>A | NCBI36 |
| NG_030442.1:g.22062G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303372.7:c.888G>A MANE Select | ENSP00000304941.5:p.Pro296= | |
| ENST00000679504.1:c.885G>A | ENSP00000505006.1:p.Pro295= | |
| ENST00000680500.1:c.888G>A | ENSP00000506438.1:p.Pro296= | |
| ENST00000680574.1:c.888G>A | ENSP00000505356.1:p.Pro296= | |
| ENST00000303372.6:c.888G>A | ENSP00000304941.5:p.Pro296= | |
| ENST00000426174.6:c.885G>A | ENSP00000395171.2:p.Pro295= | |
| NM_001143850.2:c.885G>A | NP_001137322.1:p.Pro295= | |
| NM_024809.4:c.888G>A | NP_079085.2:p.Pro296= | |
| XM_005253623.2:c.888G>A | XP_005253680.1:p.Pro296= | |
| XM_006719605.2:c.888G>A | XP_006719668.1:p.Pro296= | |
| XM_011538748.1:c.-22+1139G>A | XP_011537050.1:n.-22+1139G>A | |
| XM_006719605.3:c.888G>A | XP_006719668.1:p.Pro296= | |
| XM_017019974.1:c.885G>A | XP_016875463.1:p.Pro295= | |
| XM_017019975.1:c.-22+1139G>A | XP_016875464.1:n.-22+1139G>A | |
| NM_024809.5:c.888G>A MANE Select | NP_079085.2:p.Pro296= | |
| NM_001143850.3:c.885G>A | NP_001137322.1:p.Pro295= |