Linked Data
MyVariant Identifiers:
chr17:g.10542789A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10639472A>T , CM000679.2:g.10639472A>T | GRCh38 |
| NC_000017.10:g.10542789A>T , CM000679.1:g.10542789A>T | GRCh37 |
| NC_000017.9:g.10483514A>T | NCBI36 |
| NG_011537.1:g.22827T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000583535.6:c.2928T>A MANE Select | ENSP00000464317.1:p.Val976= | |
| ENST00000583535.5:c.2928T>A | ENSP00000464317.1:p.Val976= | |
| NM_002470.3:c.2928T>A | NP_002461.2:p.Val976= | |
| XM_011523870.1:c.2928T>A | XP_011522172.1:p.Val976= | |
| XM_011523871.1:c.2928T>A | XP_011522173.1:p.Val976= | |
| XM_011523872.1:c.2928T>A | XP_011522174.1:p.Val976= | |
| XM_011523870.3:c.2928T>A | XP_011522172.1:p.Val976= | |
| XM_011523871.2:c.2928T>A | XP_011522173.1:p.Val976= | |
| NM_002470.4:c.2928T>A MANE Select | NP_002461.2:p.Val976= |