Linked Data
gnomAD v4:
17-43952764-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43952764G>A , CM000679.2:g.43952764G>A | GRCh38 |
| NC_000017.10:g.42030132G>A , CM000679.1:g.42030132G>A | GRCh37 |
| NC_000017.9:g.39385658G>A | NCBI36 |
| NG_023338.1:g.56706C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592796.2:c.*341C>T | ENSP00000467310.1:n.*341C>T | |
| ENST00000692052.1:c.*192C>T MANE Select | ENSP00000509262.1:n.*192C>T | |
| ENST00000360085.6:c.*192C>T | ENSP00000353198.1:n.*192C>T | |
| NM_004160.4:c.*192C>T | NP_004151.3:n.*192C>T | |
| XM_011525035.1:c.*192C>T | XP_011523337.1:n.*192C>T | |
| NM_004160.5:c.*192C>T | NP_004151.3:n.*192C>T | |
| NM_001394028.1:c.*192C>T MANE Select | NP_001380957.1:n.*192C>T | |
| NM_001394029.1:c.*341C>T | NP_001380958.1:n.*341C>T | |
| NM_004160.6:c.*192C>T | NP_004151.4:n.*192C>T |