Linked Data
gnomAD v4:
7-75769692-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.75769692G>T , CM000669.2:g.75769692G>T | GRCh38 |
| NC_000007.13:g.75399010G>T , CM000669.1:g.75399010G>T | GRCh37 |
| NC_000007.12:g.75236946G>T | NCBI36 |
| NG_015989.1:g.25055C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000005180.9:c.*1C>A MANE Select | ENSP00000005180.4:n.*1C>A | |
| ENST00000005180.8:c.*1C>A | ENSP00000005180.4:n.*1C>A | |
| ENST00000394905.2:c.*1C>A | ENSP00000378365.2:n.*1C>A | |
| NM_006072.4:c.*1C>A | NP_006063.1:n.*1C>A | |
| XM_017011671.1:c.*1C>A | XP_016867160.1:n.*1C>A | |
| XM_017011672.1:c.*1C>A | XP_016867161.1:n.*1C>A | |
| NM_001371936.1:c.*1C>A | NP_001358865.1:n.*1C>A | |
| NM_001371938.1:c.*1C>A MANE Select | NP_001358867.1:n.*1C>A |