HGVS | Genome Assembly |
---|---|
NC_000019.10:g.3595492G>A , CM000681.2:g.3595492G>A | GRCh38 |
NC_000019.9:g.3595490G>A , CM000681.1:g.3595490G>A | GRCh37 |
NC_000019.8:g.3546490G>A | NCBI36 |
NG_013363.1:g.16342C>T , LRG_578:g.16342C>T | |
NG_031943.1:g.14922G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375190.10:c.*196C>T MANE Select | ENSP00000364336.4:n.*196C>T | |
ENST00000375190.8:c.*196C>T | ENSP00000364336.3:n.*196C>T | |
ENST00000411851.3:c.983+245C>T | ENSP00000393333.2:n.983+245C>T | |
ENST00000589966.1:c.*59C>T | ENSP00000468145.1:n.*59C>T | |
NM_001060.5:c.*196C>T , LRG_578t1:c.*196C>T | NP_001051.1:n.*196C>T | |
NM_201636.2:c.983+245C>T | NP_963998.2:n.983+245C>T | |
NM_001060.6:c.*196C>T MANE Select | NP_001051.1:n.*196C>T | |
NM_201636.3:c.983+245C>T | NP_963998.2:n.983+245C>T |