HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21174607A>T , CM000674.2:g.21174607A>T | GRCh38 |
NC_000012.11:g.21327541A>T , CM000674.1:g.21327541A>T | GRCh37 |
NC_000012.10:g.21218808A>T | NCBI36 |
NG_011745.1:g.48414A>T , LRG_1022:g.48414A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.257A>T MANE Select | ENSP00000256958.2:p.Tyr86Phe | |
ENST00000256958.2:c.257A>T | ENSP00000256958.2:p.Tyr86Phe | |
ENST00000543498.5:c.426-2169A>T | ||
NM_006446.4:c.257A>T , LRG_1022t1:c.257A>T | NP_006437.3:p.Tyr86Phe | |
NM_006446.5:c.257A>T MANE Select | NP_006437.3:p.Tyr86Phe |