Linked Data
MyVariant Identifiers:
chr1:g.59248278G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58782606G>T , CM000663.2:g.58782606G>T | GRCh38 |
| NC_000001.10:g.59248278G>T , CM000663.1:g.59248278G>T | GRCh37 |
| NC_000001.9:g.59020866G>T | NCBI36 |
| NG_047027.1:g.6508C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710273.1:c.531C>A | ENSP00000518166.1:p.Gly177= | |
| ENST00000371222.4:c.465C>A MANE Select | ENSP00000360266.2:p.Gly155= | |
| ENST00000678696.1:c.465C>A | ENSP00000503132.1:p.Gly155= | |
| ENST00000371222.3:c.465C>A | ENSP00000360266.2:p.Gly155= | |
| NM_002228.3:c.465C>A | NP_002219.1:p.Gly155= | |
| NM_002228.4:c.465C>A MANE Select | NP_002219.1:p.Gly155= |