Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41624184T>A , CM000679.2:g.41624184T>A | GRCh38 |
| NC_000017.10:g.39780436T>A , CM000679.1:g.39780436T>A | GRCh37 |
| NC_000017.9:g.37033962T>A | NCBI36 |
| NG_008625.1:g.5447A>T | |
| NG_009090.2:g.167529A>T , LRG_401:g.167529A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311208.13:c.326A>T MANE Select | ENSP00000308452.8:p.Asn109Ile | |
| ENST00000311208.12:c.326A>T | ENSP00000308452.8:p.Asn109Ile | |
| ENST00000463128.5:c.-290A>T | ENSP00000468672.1:n.-290A>T | |
| ENST00000491673.1:n.392A>T | ||
| ENST00000493253.5:n.113A>T | ||
| ENST00000540235.5:c.77A>T | ENSP00000441751.2:p.Asn26Ile | |
| ENST00000577817.3:c.281A>T | ENSP00000467418.1:p.Asn94Ile | |
| NM_000422.2:c.326A>T | NP_000413.1:p.Asn109Ile | |
| NM_000422.3:c.326A>T MANE Select | NP_000413.1:p.Asn109Ile |