HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94949193A>T , CM000672.2:g.94949193A>T | GRCh38 |
NC_000010.10:g.96708950A>T , CM000672.1:g.96708950A>T | GRCh37 |
NC_000010.9:g.96698940A>T | NCBI36 |
NG_008385.1:g.15536A>T | |
NG_008385.2:g.16036A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.728A>T MANE Select | ENSP00000260682.6:p.Tyr243Phe | |
ENST00000643112.1:c.728A>T | ENSP00000496202.1:p.Tyr243Phe | |
ENST00000260682.6:c.728A>T | ENSP00000260682.6:p.Tyr243Phe | |
ENST00000473496.1:n.499A>T | ||
NM_000771.3:c.728A>T | NP_000762.2:p.Tyr243Phe | |
NM_000771.4:c.728A>T MANE Select | NP_000762.2:p.Tyr243Phe |