HGVS | Genome Assembly |
---|---|
NC_000010.11:g.80280503C= , CM000672.2:g.80280503C= | GRCh38 |
NC_000010.10:g.82040259C= , CM000672.1:g.82040259C= | GRCh37 |
NC_000010.9:g.82030239C= | NCBI36 |
NG_008083.1:g.14176G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372213.8:c.405+177G= MANE Select | ENSP00000361287.3:n.405+177G= | |
ENST00000372213.7:c.405+177G= | ENSP00000361287.3:n.405+177G= | |
ENST00000455001.1:c.216+177G= | ENSP00000414961.1:n.216+177G= | |
NM_000429.2:c.405+177G= | NP_000420.1:n.405+177G= | |
XM_005269842.3:c.405+177G= | XP_005269899.1:n.405+177G= | |
XM_005269843.3:c.282+177G= | XP_005269900.1:n.282+177G= | |
NM_000429.3:c.405+177G= MANE Select | NP_000420.1:n.405+177G= |