HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6714513G= , CM000681.2:g.6714513G= | GRCh38 |
NC_000019.9:g.6714524G= , CM000681.1:g.6714524G= | GRCh37 |
NC_000019.8:g.6665524G= | NCBI36 |
NG_009557.1:g.11139C= , LRG_27:g.11139C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.382-67C= | ENSP00000512083.1:n.382-67C= | |
ENST00000245907.11:c.505-67C= MANE Select | ENSP00000245907.4:n.505-67C= | |
ENST00000245907.10:c.505-67C= | ENSP00000245907.4:n.505-67C= | |
NM_000064.3:c.505-67C= | NP_000055.2:n.505-67C= | |
NM_000064.4:c.505-67C= MANE Select | NP_000055.2:n.505-67C= |