Linked Data
MyVariant Identifiers:
chr1:g.59248302T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58782630T>A , CM000663.2:g.58782630T>A | GRCh38 |
| NC_000001.10:g.59248302T>A , CM000663.1:g.59248302T>A | GRCh37 |
| NC_000001.9:g.59020890T>A | NCBI36 |
| NG_047027.1:g.6484A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710273.1:c.507A>T | ENSP00000518166.1:p.Val169= | |
| ENST00000371222.4:c.441A>T MANE Select | ENSP00000360266.2:p.Val147= | |
| ENST00000678696.1:c.441A>T | ENSP00000503132.1:p.Val147= | |
| ENST00000371222.3:c.441A>T | ENSP00000360266.2:p.Val147= | |
| NM_002228.3:c.441A>T | NP_002219.1:p.Val147= | |
| NM_002228.4:c.441A>T MANE Select | NP_002219.1:p.Val147= |