HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157241676G>T , CM000667.2:g.157241676G>T | GRCh38 |
NC_000005.9:g.156668686G>T , CM000667.1:g.156668686G>T | GRCh37 |
NC_000005.8:g.156601264G>T | NCBI36 |
NG_016276.1:g.65780G>T , LRG_189:g.65780G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696962.1:c.882G>T | ENSP00000513001.1:p.Leu294Phe | |
ENST00000422843.8:c.1016G>T MANE Select | ENSP00000398655.4:p.Cys339Phe | |
ENST00000422843.7:c.1016G>T | ENSP00000398655.3:p.Cys339Phe | |
ENST00000519402.5:n.2601G>T | ||
ENST00000519749.1:n.86G>T | ||
ENST00000520173.1:n.134G>T | ||
NM_005546.3:c.1016G>T , LRG_189t1:c.1016G>T | NP_005537.3:p.Cys339Phe | |
XM_017009443.1:c.641G>T | XP_016864932.1:p.Cys214Phe | |
NM_005546.4:c.1016G>T MANE Select | NP_005537.3:p.Cys339Phe |