Linked Data
gnomAD v4:
20-46011298-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011298G>T , CM000682.2:g.46011298G>T | GRCh38 |
| NC_000020.10:g.44639937G>T , CM000682.1:g.44639937G>T | GRCh37 |
| NC_000020.9:g.44073344G>T | NCBI36 |
| NG_011468.1:g.7391G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.805G>T MANE Select | ENSP00000361405.3:p.Gly269Cys | |
| NM_004994.2:c.805G>T | NP_004985.2:p.Gly269Cys | |
| NM_004994.3:c.805G>T MANE Select | NP_004985.2:p.Gly269Cys |