Linked Data
ClinVar Variation Id:
6336
ClinVar RCV Id:
RCV001851704
dbSNP Id:
rs121908647
gnomAD v2:
9-133370368-G-T
gnomAD v4:
9-130494981-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130494981G>T , CM000671.2:g.130494981G>T | GRCh38 |
| NC_000009.11:g.133370368G>T , CM000671.1:g.133370368G>T | GRCh37 |
| NC_000009.10:g.132360189G>T | NCBI36 |
| NG_011542.1:g.55275G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000352480.10:c.1085G>T MANE Select | ENSP00000253004.6:p.Gly362Val | |
| ENST00000352480.9:c.1085G>T | ENSP00000253004.6:p.Gly362Val | |
| ENST00000372386.6:n.356G>T | ||
| ENST00000372393.7:c.1085G>T | ENSP00000361469.2:p.Gly362Val | |
| ENST00000372394.5:c.1085G>T | ENSP00000361471.1:p.Gly362Val | |
| NM_000050.4:c.1085G>T | NP_000041.2:p.Gly362Val | |
| NM_054012.3:c.1085G>T | NP_446464.1:p.Gly362Val | |
| XM_005272200.2:c.1085G>T | XP_005272257.1:p.Gly362Val | |
| XM_011518705.1:c.1199G>T | XP_011517007.1:p.Gly400Val | |
| XR_930393.1:n.1060-2724C>A | ||
| XM_005272200.3:c.1085G>T | XP_005272257.1:p.Gly362Val | |
| XM_011518705.2:c.1199G>T | XP_011517007.1:p.Gly400Val | |
| XM_017014729.1:c.1181G>T | XP_016870218.1:p.Gly394Val | |
| XR_930393.2:n.1102-2724C>A | ||
| NM_054012.4:c.1085G>T MANE Select | NP_446464.1:p.Gly362Val |