HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15191895A= , CM000681.2:g.15191895A= | GRCh38 |
NC_000019.9:g.15302706A= , CM000681.1:g.15302706A= | GRCh37 |
NC_000019.8:g.15163706A= | NCBI36 |
NG_009819.1:g.14087T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.680-28T= MANE Select | ENSP00000263388.1:n.680-28T= | |
ENST00000263388.6:c.680-28T= | ENSP00000263388.1:n.680-28T= | |
ENST00000601011.1:c.677-28T= | ENSP00000473138.1:n.677-28T= | |
NM_000435.2:c.680-28T= | NP_000426.2:n.680-28T= | |
XM_005259924.3:c.680-28T= | XP_005259981.1:n.680-28T= | |
XM_005259924.4:c.680-28T= | XP_005259981.1:n.680-28T= | |
NM_000435.3:c.680-28T= MANE Select | NP_000426.2:n.680-28T= |