Linked Data
ClinVar Variation Id:
516372
dbSNP Id:
rs774605205
ExAC:
8:134251151 G / A
gnomAD v2:
8-134251151-G-A
gnomAD v3:
8-133238908-G-A
gnomAD v4:
8-133238908-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.133238908G>A , CM000670.2:g.133238908G>A | GRCh38 |
| NC_000008.10:g.134251151G>A , CM000670.1:g.134251151G>A | GRCh37 |
| NC_000008.9:g.134320333G>A | NCBI36 |
| NG_007943.1:g.63348C>T , LRG_258:g.63348C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000323851.13:c.1155C>T MANE Select | ENSP00000319977.8:p.Ala385= | |
| ENST00000537882.3:c.1155C>T | ENSP00000437443.2:p.Ala385= | |
| ENST00000323851.11:c.1155C>T | ENSP00000319977.7:p.Ala385= | |
| ENST00000414097.6:c.1155C>T | ENSP00000404854.2:p.Ala385= | |
| ENST00000517599.5:c.*761C>T | ENSP00000429172.1:n.*761C>T | |
| ENST00000518066.5:c.282C>T | ENSP00000431057.1:p.Ala94= | |
| ENST00000518176.5:c.396C>T | ENSP00000429007.1:p.Ala132= | |
| ENST00000519278.5:n.2251C>T | ||
| ENST00000521026.5:n.413C>T | ||
| ENST00000521414.5:n.617C>T | ||
| ENST00000521438.1:n.2456+164C>T | ||
| ENST00000522476.5:c.957C>T | ENSP00000427894.1:p.Ala319= | |
| ENST00000537882.2:c.912C>T | ENSP00000437443.1:p.Ala304= | |
| NM_001135242.1:c.1155C>T | NP_001128714.1:p.Ala385= | |
| NM_001258432.1:c.957C>T | NP_001245361.1:p.Ala319= | |
| NM_001258433.1:c.912C>T | NP_001245362.1:p.Ala304= | |
| NM_006096.3:c.1155C>T , LRG_258t1:c.1155C>T | NP_006087.2:p.Ala385= | |
| XM_011516791.1:c.1206C>T | XP_011515093.1:p.Ala402= | |
| XM_011516792.1:c.588C>T | XP_011515094.1:p.Ala196= | |
| XM_011516792.2:c.588C>T | XP_011515094.1:p.Ala196= | |
| NM_001135242.2:c.1155C>T | NP_001128714.1:p.Ala385= | |
| NM_001258432.2:c.957C>T | NP_001245361.1:p.Ala319= | |
| NM_001258433.2:c.912C>T | NP_001245362.1:p.Ala304= | |
| NM_001374844.1:c.1206C>T | NP_001361773.1:p.Ala402= | |
| NM_001374845.1:c.1155C>T | NP_001361774.1:p.Ala385= | |
| NM_001374846.1:c.1155C>T | NP_001361775.1:p.Ala385= | |
| NM_001374847.1:c.957C>T | NP_001361776.1:p.Ala319= | |
| NM_006096.4:c.1155C>T MANE Select | NP_006087.2:p.Ala385= |