HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177993134G= , CM000667.2:g.177993134G= | GRCh38 |
NC_000005.9:g.177420135G= , CM000667.1:g.177420135G= | GRCh37 |
NC_000005.8:g.177352741G= | NCBI36 |
NG_015889.1:g.8109C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.343-87C= MANE Select | ENSP00000311290.2:n.343-87C= | |
NM_006261.4:c.343-87C= | NP_006252.3:n.343-87C= | |
NM_006261.5:c.343-87C= MANE Select | NP_006252.4:n.343-87C= |