HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21002094A>T , CM000664.2:g.21002094A>T | GRCh38 |
NC_000002.11:g.21224966A>T , CM000664.1:g.21224966A>T | GRCh37 |
NC_000002.10:g.21078471A>T | NCBI36 |
NG_011793.1:g.46980T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.13328T>A MANE Select | ENSP00000233242.1:p.Phe4443Tyr | |
ENST00000616098.4:c.13326T>A | ENSP00000477990.1:n.13326T>A | |
NM_000384.2:c.13328T>A | NP_000375.2:p.Phe4443Tyr | |
XM_011532809.1:c.5870-2821T>A | XP_011531111.1:n.5870-2821T>A | |
NM_000384.3:c.13328T>A MANE Select | NP_000375.3:p.Phe4443Tyr |