HGVS | Genome Assembly |
---|---|
NC_000001.11:g.203183584C= , CM000663.2:g.203183584C= | GRCh38 |
NC_000001.10:g.203152712C= , CM000663.1:g.203152712C= | GRCh37 |
NC_000001.9:g.201419335C= | NCBI36 |
NG_013056.1:g.8211G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000255409.8:c.465+57G= MANE Select | ENSP00000255409.3:n.465+57G= | |
ENST00000255409.7:c.465+57G= | ENSP00000255409.3:n.465+57G= | |
NM_001276.2:c.465+57G= | NP_001267.2:n.465+57G= | |
XM_011509105.1:c.483+57G= | XP_011507407.1:n.483+57G= | |
XM_011509106.1:c.483+57G= | XP_011507408.1:n.483+57G= | |
XM_011509107.1:c.465+57G= | XP_011507409.1:n.465+57G= | |
XM_011509108.1:c.483+57G= | XP_011507410.1:n.483+57G= | |
NM_001276.3:c.465+57G= | NP_001267.2:n.465+57G= | |
NM_001276.4:c.465+57G= MANE Select | NP_001267.2:n.465+57G= |