HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1535772A>C , CM000663.2:g.1535772A>C | GRCh38 |
NC_000001.10:g.1471152A>C , CM000663.1:g.1471152A>C | GRCh37 |
NC_000001.9:g.1461015A>C | NCBI36 |
NG_041807.1:g.9589T>G | |
NG_053035.1:g.28630A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378733.9:c.190T>G MANE Select | ENSP00000368007.4:p.Tyr64Asp | |
ENST00000378733.8:c.190T>G | ENSP00000368007.4:p.Tyr64Asp | |
ENST00000425828.1:c.190T>G | ENSP00000400311.1:p.Tyr64Asp | |
NM_001114748.1:c.190T>G | NP_001108220.1:p.Tyr64Asp | |
NM_001114748.2:c.190T>G MANE Select | NP_001108220.1:p.Tyr64Asp |