HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62020036C= , CM000672.2:g.62020036C= | GRCh38 |
NC_000010.10:g.63779795C= , CM000672.1:g.63779795C= | GRCh37 |
NC_000010.9:g.63449801C= | NCBI36 |
NG_030027.1:g.123783C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000279873.12:c.733+19715C= MANE Select | ENSP00000279873.7:n.733+19715C= | |
ENST00000644638.1:c.734-4637C= | ENSP00000494412.1:n.734-4637C= | |
ENST00000681100.1:c.733+19715C= | ENSP00000506119.1:n.733+19715C= | |
ENST00000279873.11:c.733+19715C= | ENSP00000279873.7:n.733+19715C= | |
NM_032199.2:c.733+19715C= | NP_115575.1:n.733+19715C= | |
XM_011540262.1:c.503-30852C= | XP_011538564.1:n.503-30852C= | |
XM_024448230.1:c.166+19715C= | XP_024303998.1:n.166+19715C= | |
NM_032199.3:c.733+19715C= MANE Select | NP_115575.1:n.733+19715C= |