HGVS | Genome Assembly |
---|---|
NC_000010.11:g.100045648G>A , CM000672.2:g.100045648G>A | GRCh38 |
NC_000010.10:g.101805405G>A , CM000672.1:g.101805405G>A | GRCh37 |
NC_000010.9:g.101795395G>A | NCBI36 |
NG_012060.1:g.41238C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370418.8:c.1231-3075C>T MANE Select | ENSP00000359446.3:n.1231-3075C>T | |
ENST00000370418.7:c.1231-3075C>T | ENSP00000359446.3:n.1231-3075C>T | |
NM_001308.2:c.1231-3075C>T | NP_001299.1:n.1231-3075C>T | |
XM_011539299.1:c.1273-3075C>T | XP_011537601.1:n.1273-3075C>T | |
NM_001308.3:c.1231-3075C>T MANE Select | NP_001299.1:n.1231-3075C>T |