Linked Data
gnomAD v4:
8-37966011-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37966011G>T , CM000670.2:g.37966011G>T | GRCh38 |
| NC_000008.10:g.37823529G>T , CM000670.1:g.37823529G>T | GRCh37 |
| NC_000008.9:g.37942686G>T | NCBI36 |
| NG_011936.1:g.5656C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000345060.5:c.459C>A MANE Select | ENSP00000343782.3:p.Cys153Ter | |
| ENST00000520341.2:n.587C>A | ||
| ENST00000345060.4:c.459C>A | ENSP00000343782.3:p.Cys153Ter | |
| ENST00000614635.1:c.459C>A | ENSP00000480325.1:p.Cys153Ter | |
| NM_000025.2:c.459C>A | NP_000016.1:p.Cys153Ter | |
| NM_000025.3:c.459C>A MANE Select | NP_000016.1:p.Cys153Ter |