Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.208129652C>A , CM000664.2:g.208129652C>A | GRCh38 |
| NC_000002.11:g.208994376C>A , CM000664.1:g.208994376C>A | GRCh37 |
| NC_000002.10:g.208702621C>A | NCBI36 |
| NG_008038.1:g.5179G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282141.4:c.41G>T MANE Select | ENSP00000282141.3:p.Gly14Val | |
| ENST00000282141.3:c.41G>T | ENSP00000282141.3:p.Gly14Val | |
| NM_020989.3:c.41G>T | NP_066269.1:p.Gly14Val | |
| NR_038437.1:n.98-7404C>A | ||
| XM_011510661.1:c.41G>T | XP_011508963.1:p.Gly14Val | |
| XM_011510662.1:c.41G>T | XP_011508964.1:p.Gly14Val | |
| XM_011510663.1:c.-89G>T | XP_011508965.1:n.-89G>T | |
| NM_020989.4:c.41G>T MANE Select | NP_066269.1:p.Gly14Val |