MyVariant.info:
GRCh37
chr3:g.87311311G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.87262161G>T , CM000665.2:g.87262161G>T | GRCh38 |
| NC_000003.11:g.87311311G>T , CM000665.1:g.87311311G>T | GRCh37 |
| NC_000003.10:g.87394001G>T | NCBI36 |
| NG_008225.2:g.19427C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344265.8:c.592C>A | ENSP00000342931.3:p.Arg198= | |
| ENST00000350375.7:c.514C>A MANE Select | ENSP00000263781.2:p.Arg172= | |
| ENST00000344265.7:c.592C>A | ENSP00000342931.3:p.Arg198= | |
| ENST00000350375.6:c.514C>A | ENSP00000263781.2:p.Arg172= | |
| ENST00000560656.1:c.440-2057C>A | ENSP00000452610.1:n.440-2057C>A | |
| ENST00000561167.5:c.289C>A | ENSP00000454072.1:p.Arg97= | |
| NM_000306.3:c.514C>A | NP_000297.1:p.Arg172= | |
| NM_001122757.2:c.592C>A | NP_001116229.1:p.Arg198= | |
| NM_000306.4:c.514C>A MANE Select | NP_000297.1:p.Arg172= | |
| NM_001122757.3:c.592C>A | NP_001116229.1:p.Arg198= |