Linked Data
gnomAD v4:
X-8731966-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8731966G>A , CM000685.2:g.8731966G>A | GRCh38 |
| NC_000023.10:g.8700007G>A , CM000685.1:g.8700007G>A | GRCh37 |
| NC_000023.9:g.8660007G>A | NCBI36 |
| NG_007088.1:g.5221C>T | |
| NG_007088.2:g.5221C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262648.8:c.71C>T MANE Select | ENSP00000262648.3:p.Ala24Val | |
| ENST00000262648.7:c.71C>T | ENSP00000262648.3:p.Ala24Val | |
| ENST00000619786.1:c.70C>T | ENSP00000478734.1:p.Arg24Trp | |
| NM_000216.2:c.71C>T | NP_000207.2:p.Ala24Val | |
| XM_005274501.3:c.71C>T | XP_005274558.1:p.Ala24Val | |
| NM_000216.3:c.71C>T | NP_000207.2:p.Ala24Val | |
| XM_005274501.4:c.71C>T | XP_005274558.1:p.Ala24Val | |
| NM_000216.4:c.71C>T MANE Select | NP_000207.2:p.Ala24Val |