Linked Data
gnomAD v4:
1-58576783-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58576783C>T , CM000663.2:g.58576783C>T | GRCh38 |
| NC_000001.10:g.59042455C>T , CM000663.1:g.59042455C>T | GRCh37 |
| NC_000001.9:g.58815043C>T | NCBI36 |
| NG_016237.1:g.5712G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371225.4:c.374G>A MANE Select | ENSP00000360269.2:p.Cys125Tyr | |
| ENST00000371225.3:c.374G>A | ENSP00000360269.2:p.Cys125Tyr | |
| NM_002353.2:c.374G>A | NP_002344.2:p.Cys125Tyr | |
| NM_002353.3:c.374G>A MANE Select | NP_002344.2:p.Cys125Tyr |