HGVS | Genome Assembly |
---|---|
NC_000019.10:g.3595596C= , CM000681.2:g.3595596C= | GRCh38 |
NC_000019.9:g.3595594C= , CM000681.1:g.3595594C= | GRCh37 |
NC_000019.8:g.3546594C= | NCBI36 |
NG_013363.1:g.16238G= , LRG_578:g.16238G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375190.10:c.*92G= MANE Select | ENSP00000364336.4:n.*92G= | |
ENST00000375190.8:c.*92G= | ENSP00000364336.3:n.*92G= | |
ENST00000411851.3:c.983+141G= | ENSP00000393333.2:n.983+141G= | |
ENST00000589966.1:c.735G= | ENSP00000468145.1:p.Gly245= | |
NM_001060.5:c.*92G= , LRG_578t1:c.*92G= | NP_001051.1:n.*92G= | |
NM_201636.2:c.983+141G= | NP_963998.2:n.983+141G= | |
XM_011528214.2:c.*92G= | XP_011526516.1:n.*92G= | |
NM_001060.6:c.*92G= MANE Select | NP_001051.1:n.*92G= | |
NM_201636.3:c.983+141G= | NP_963998.2:n.983+141G= |