HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571275A>T , CM000663.2:g.154571275A>T | GRCh38 |
NC_000001.10:g.154543751A>T , CM000663.1:g.154543751A>T | GRCh37 |
NC_000001.9:g.152810375A>T | NCBI36 |
NG_008027.1:g.8495A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.452A>T MANE Select | ENSP00000357461.3:p.Tyr151Phe | |
ENST00000636034.1:c.452A>T | ENSP00000489703.1:p.Tyr151Phe | |
ENST00000637900.1:c.458A>T | ENSP00000490474.1:p.Tyr153Phe | |
ENST00000368476.3:c.452A>T | ENSP00000357461.3:p.Tyr151Phe | |
NM_000748.2:c.452A>T | NP_000739.1:p.Tyr151Phe | |
XM_017000180.2:c.-9-50A>T | XP_016855669.1:n.-9-50A>T | |
XR_001736952.2:n.704A>T | ||
NM_000748.3:c.452A>T MANE Select | NP_000739.1:p.Tyr151Phe |