Linked Data
ClinVar Variation Id:
230545
dbSNP Id:
rs876658624
gnomAD v2:
13-32931930-G-A
gnomAD v3:
13-32357793-G-A
gnomAD v4:
13-32357793-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32357793G>A , CM000675.2:g.32357793G>A | GRCh38 |
| NC_000013.10:g.32931930G>A , CM000675.1:g.32931930G>A | GRCh37 |
| NC_000013.9:g.31829930G>A | NCBI36 |
| NG_012772.3:g.47314G>A , LRG_293:g.47314G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000470094.2:c.7669G>A | ENSP00000434898.2:p.Ala2557Thr | |
| ENST00000528762.2:c.7669G>A | ENSP00000433168.2:p.Ala2557Thr | |
| ENST00000530893.7:c.7300G>A | ENSP00000499438.2:p.Ala2434Thr | |
| ENST00000665585.2:c.7669G>A | ENSP00000499570.2:p.Ala2557Thr | |
| ENST00000666593.2:c.7669G>A | ENSP00000499256.2:p.Ala2557Thr | |
| ENST00000700202.2:c.7669G>A | ENSP00000514856.2:p.Ala2557Thr | |
| ENST00000700202.1:c.136G>A | ENSP00000514856.1:p.Ala46Thr | |
| ENST00000380152.8:c.7669G>A MANE Select | ENSP00000369497.3:p.Ala2557Thr | |
| ENST00000544455.6:c.7669G>A | ENSP00000439902.1:p.Ala2557Thr | |
| ENST00000614259.2:c.7669G>A | ENSP00000506251.1:p.Ala2557Thr | |
| ENST00000665585.1:c.234G>A | ||
| ENST00000680887.1:c.7669G>A | ENSP00000505508.1:p.Ala2557Thr | |
| ENST00000380152.7:c.7669G>A | ENSP00000369497.3:p.Ala2557Thr | |
| ENST00000544455.5:c.7669G>A | ENSP00000439902.1:p.Ala2557Thr | |
| ENST00000614259.1:n.7669G>A | ||
| NM_000059.3:c.7669G>A , LRG_293t1:c.7669G>A | NP_000050.2:p.Ala2557Thr | |
| XM_011535203.1:c.7669G>A | XP_011533505.1:p.Ala2557Thr | |
| XM_011535204.1:c.7573G>A | XP_011533506.1:p.Ala2525Thr | |
| XM_011535205.1:c.7669G>A | XP_011533507.1:p.Ala2557Thr | |
| NM_000059.4:c.7669G>A MANE Select | NP_000050.3:p.Ala2557Thr |