Linked Data
gnomAD v4:
7-155463325-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.155463325C>T , CM000669.2:g.155463325C>T | GRCh38 |
| NC_000007.13:g.155256020C>T , CM000669.1:g.155256020C>T | GRCh37 |
| NC_000007.12:g.154948781C>T | NCBI36 |
| NG_007124.1:g.11606C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297375.4:c.*638C>T MANE Select | ENSP00000297375.4:n.*638C>T | |
| NM_001427.3:c.*638C>T | NP_001418.2:n.*638C>T | |
| NM_001427.4:c.*638C>T MANE Select | NP_001418.2:n.*638C>T |