Linked Data
ClinVar Variation Id:
410920
dbSNP Id:
rs201458896
ExAC:
13:48954347 G / A
gnomAD v2:
13-48954347-G-A
gnomAD v3:
13-48380211-G-A
gnomAD v4:
13-48380211-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48380211G>A , CM000675.2:g.48380211G>A | GRCh38 |
| NC_000013.10:g.48954347G>A , CM000675.1:g.48954347G>A | GRCh37 |
| NC_000013.9:g.47852348G>A | NCBI36 |
| NG_009009.1:g.81465G>A , LRG_517:g.81465G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.1468G>A MANE Select | ENSP00000267163.4:p.Ala490Thr | |
| ENST00000650461.1:c.1468G>A | ENSP00000497193.1:p.Ala490Thr | |
| ENST00000267163.4:c.1468G>A | ENSP00000267163.4:p.Ala490Thr | |
| NM_000321.2:c.1468G>A , LRG_517t1:c.1468G>A | NP_000312.2:p.Ala490Thr | |
| XM_011535171.1:c.1207G>A | XP_011533473.1:p.Ala403Thr | |
| XM_011535171.2:c.1207G>A | XP_011533473.1:p.Ala403Thr | |
| NM_000321.3:c.1468G>A MANE Select | NP_000312.2:p.Ala490Thr |