HGVS | Genome Assembly |
---|---|
NC_000019.10:g.3595366A>T , CM000681.2:g.3595366A>T | GRCh38 |
NC_000019.9:g.3595364A>T , CM000681.1:g.3595364A>T | GRCh37 |
NC_000019.8:g.3546364A>T | NCBI36 |
NG_013363.1:g.16468T>A , LRG_578:g.16468T>A | |
NG_031943.1:g.14796A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375190.10:c.*322T>A MANE Select | ENSP00000364336.4:n.*322T>A | |
ENST00000375190.8:c.*322T>A | ENSP00000364336.3:n.*322T>A | |
ENST00000411851.3:c.984-290T>A | ENSP00000393333.2:n.984-290T>A | |
ENST00000589966.1:c.*185T>A | ENSP00000468145.1:n.*185T>A | |
NM_001060.5:c.*322T>A , LRG_578t1:c.*322T>A | NP_001051.1:n.*322T>A | |
NM_201636.2:c.984-290T>A | NP_963998.2:n.984-290T>A | |
NM_001060.6:c.*322T>A MANE Select | NP_001051.1:n.*322T>A | |
NM_201636.3:c.984-290T>A | NP_963998.2:n.984-290T>A |