Linked Data
gnomAD v4:
14-23414999-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23414999T>C , CM000676.2:g.23414999T>C | GRCh38 |
| NC_000014.8:g.23884208T>C , CM000676.1:g.23884208T>C | GRCh37 |
| NC_000014.7:g.22954048T>C | NCBI36 |
| NG_007884.1:g.25663A>G , LRG_384:g.25663A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.5555A>G MANE Select | ENSP00000347507.3:p.Tyr1852Cys | |
| ENST00000355349.3:c.5555A>G | ENSP00000347507.3:p.Tyr1852Cys | |
| NM_000257.3:c.5555A>G | NP_000248.2:p.Tyr1852Cys | |
| XM_017021340.1:c.5555A>G | XP_016876829.1:p.Tyr1852Cys | |
| NM_000257.4:c.5555A>G MANE Select | NP_000248.2:p.Tyr1852Cys |