HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65239790T>A , CM000674.2:g.65239790T>A | GRCh38 |
NC_000012.11:g.65633570T>A , CM000674.1:g.65633570T>A | GRCh37 |
NC_000012.10:g.63919837T>A | NCBI36 |
NG_016210.1:g.75220T>A | |
NG_016210.2:g.75220T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.1922-139T>A MANE Select | ENSP00000308369.2:n.1922-139T>A | |
ENST00000308330.2:c.1922-139T>A | ENSP00000308369.2:n.1922-139T>A | |
NM_001167614.1:c.1919-139T>A | NP_001161086.1:n.1919-139T>A | |
NM_014319.4:c.1922-139T>A | NP_055134.2:n.1922-139T>A | |
NM_014319.5:c.1922-139T>A MANE Select | NP_055134.2:n.1922-139T>A | |
NM_001167614.2:c.1919-139T>A | NP_001161086.1:n.1919-139T>A |