HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115033511A>T , CM000663.2:g.115033511A>T | GRCh38 |
NC_000001.10:g.115576132A>T , CM000663.1:g.115576132A>T | GRCh37 |
NC_000001.9:g.115377655A>T | NCBI36 |
NG_015891.1:g.8718A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256592.3:c.149A>T MANE Select | ENSP00000256592.1:p.Tyr50Phe | |
ENST00000256592.2:c.149A>T | ENSP00000256592.1:p.Tyr50Phe | |
ENST00000369517.1:c.149A>T | ENSP00000358530.1:p.Tyr50Phe | |
NM_000549.4:c.149A>T | NP_000540.2:p.Tyr50Phe | |
XM_011542065.1:c.149A>T | XP_011540367.1:p.Tyr50Phe | |
XM_011542065.2:c.149A>T | XP_011540367.1:p.Tyr50Phe | |
NM_000549.5:c.149A>T MANE Select | NP_000540.2:p.Tyr50Phe |