Linked Data
ClinVar Variation Id:
360442
dbSNP Id:
rs11575290
ExAC:
7:50611688 G / A
gnomAD v2:
7-50611688-G-A
gnomAD v3:
7-50543990-G-A
gnomAD v4:
7-50543990-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.50543990G>A , CM000669.2:g.50543990G>A | GRCh38 |
| NC_000007.13:g.50611688G>A , CM000669.1:g.50611688G>A | GRCh37 |
| NC_000007.12:g.50579182G>A | NCBI36 |
| NG_008742.1:g.26467C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000444124.7:c.96C>T MANE Select | ENSP00000403644.2:p.Asp32= | |
| ENST00000357936.9:c.96C>T | ENSP00000350616.5:p.Asp32= | |
| ENST00000380984.4:c.96C>T | ENSP00000370371.4:p.Asp32= | |
| ENST00000426377.5:c.96C>T | ENSP00000395069.1:p.Asp32= | |
| ENST00000431062.5:c.96C>T | ENSP00000399184.1:p.Asp32= | |
| ENST00000444124.6:c.96C>T | ENSP00000403644.2:p.Asp32= | |
| ENST00000444733.5:c.96C>T | ENSP00000393724.1:p.Asp32= | |
| ENST00000615193.4:c.96C>T | ENSP00000484104.1:p.Asp32= | |
| ENST00000617822.4:c.96C>T | ENSP00000478385.1:p.Asp32= | |
| ENST00000622873.4:c.96C>T | ENSP00000479110.1:p.Asp32= | |
| NM_000790.3:c.96C>T | NP_000781.1:p.Asp32= | |
| NM_001082971.1:c.96C>T | NP_001076440.1:p.Asp32= | |
| NM_001242886.1:c.96C>T | NP_001229815.1:p.Asp32= | |
| NM_001242887.1:c.96C>T | NP_001229816.1:p.Asp32= | |
| NM_001242888.1:c.96C>T | NP_001229817.1:p.Asp32= | |
| NM_001242889.1:c.96C>T | NP_001229818.1:p.Asp32= | |
| NM_001242890.1:c.96C>T | NP_001229819.1:p.Asp32= | |
| XM_005271745.3:c.96C>T | XP_005271802.1:p.Asp32= | |
| XM_005271745.4:c.96C>T | XP_005271802.1:p.Asp32= | |
| NM_001082971.2:c.96C>T MANE Select | NP_001076440.2:p.Asp32= | |
| NM_000790.4:c.96C>T | NP_000781.2:p.Asp32= | |
| NM_001242888.2:c.96C>T | NP_001229817.2:p.Asp32= | |
| NM_001242890.2:c.96C>T | NP_001229819.2:p.Asp32= | |
| NM_001242886.2:c.96C>T | NP_001229815.2:p.Asp32= | |
| NM_001242887.2:c.96C>T | NP_001229816.2:p.Asp32= | |
| NM_001242889.2:c.96C>T | NP_001229818.2:p.Asp32= |