Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6112274T>A , CM000663.2:g.6112274T>A | GRCh38 |
| NC_000001.10:g.6172334T>A , CM000663.1:g.6172334T>A | GRCh37 |
| NC_000001.9:g.6094921T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262450.8:c.5006A>T MANE Select | ENSP00000262450.3:p.Asp1669Val | |
| ENST00000262450.7:c.5006A>T | ENSP00000262450.3:p.Asp1669Val | |
| ENST00000377999.5:c.1909A>T | ENSP00000367238.2:n.1909A>T | |
| ENST00000462991.5:c.3259A>T | ||
| ENST00000496404.1:c.3724A>T | ENSP00000433676.1:n.3724A>T | |
| NM_015557.2:c.5006A>T | NP_056372.1:p.Asp1669Val | |
| NM_015557.3:c.5006A>T MANE Select | NP_056372.1:p.Asp1669Val |