Linked Data
dbSNP Id:
rs749388940
ExAC:
3:119121123 G / A
gnomAD v2:
3-119121123-G-A
gnomAD v4:
3-119402276-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119402276G>A , CM000665.2:g.119402276G>A | GRCh38 |
| NC_000003.11:g.119121123G>A , CM000665.1:g.119121123G>A | GRCh37 |
| NC_000003.10:g.120603813G>A | NCBI36 |
| NG_007665.2:g.112904G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.1524G>A MANE Select | ENSP00000264245.4:p.Pro508= | |
| ENST00000264245.8:c.1524G>A | ENSP00000264245.4:p.Pro508= | |
| NM_020754.3:c.1524G>A | NP_065805.2:p.Pro508= | |
| XM_005247671.3:c.1431G>A | XP_005247728.1:p.Pro477= | |
| XM_006713714.2:c.1464G>A | XP_006713777.1:p.Pro488= | |
| XM_006713714.3:c.1464G>A | XP_006713777.1:p.Pro488= | |
| XM_017006955.1:c.1032G>A | XP_016862444.1:p.Pro344= | |
| NM_020754.4:c.1524G>A MANE Select | NP_065805.2:p.Pro508= |