Linked Data
gnomAD v4:
13-27924271-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924271C>T , CM000675.2:g.27924271C>T | GRCh38 |
| NC_000013.10:g.28498408C>T , CM000675.1:g.28498408C>T | GRCh37 |
| NC_000013.9:g.27396408C>T | NCBI36 |
| NG_008183.1:g.9241C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.422C>T MANE Select | ENSP00000370421.4:p.Ala141Val | |
| ENST00000381033.4:c.422C>T | ENSP00000370421.4:p.Ala141Val | |
| NM_000209.3:c.422C>T | NP_000200.1:p.Ala141Val | |
| XR_941578.1:n.3549C>T | ||
| XR_941579.1:n.2148C>T | ||
| XR_941580.1:n.1064C>T | ||
| XR_941578.2:n.3561C>T | ||
| XR_941580.2:n.1076C>T | ||
| NM_000209.4:c.422C>T MANE Select | NP_000200.1:p.Ala141Val |