HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21001950T>A , CM000664.2:g.21001950T>A | GRCh38 |
NC_000002.11:g.21224822T>A , CM000664.1:g.21224822T>A | GRCh37 |
NC_000002.10:g.21078327T>A | NCBI36 |
NG_011793.1:g.47124A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.13472A>T MANE Select | ENSP00000233242.1:p.Tyr4491Phe | |
ENST00000616098.4:c.13470A>T | ENSP00000477990.1:n.13470A>T | |
NM_000384.2:c.13472A>T | NP_000375.2:p.Tyr4491Phe | |
XM_011532809.1:c.5870-2677A>T | XP_011531111.1:n.5870-2677A>T | |
NM_000384.3:c.13472A>T MANE Select | NP_000375.3:p.Tyr4491Phe |