HGVS | Genome Assembly |
---|---|
NC_000011.10:g.13974453A= , CM000673.2:g.13974453A= | GRCh38 |
NC_000011.9:g.13996000A= , CM000673.1:g.13996000A= | GRCh37 |
NC_000011.8:g.13952576A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000576479.4:c.239-8394A= MANE Select | ENSP00000460236.1:n.239-8394A= | |
ENST00000576479.3:c.239-8394A= | ENSP00000460236.1:n.239-8394A= | |
NM_006108.3:c.239-8394A= | NP_006099.2:n.239-8394A= | |
NM_006108.4:c.239-8394A= MANE Select | NP_006099.2:n.239-8394A= |