HGVS | Genome Assembly |
---|---|
NC_000006.12:g.131861621C= , CM000668.2:g.131861621C= | GRCh38 |
NC_000006.11:g.132182761C= , CM000668.1:g.132182761C= | GRCh37 |
NC_000006.10:g.132224454C= | NCBI36 |
NG_008206.1:g.58606C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647893.1:c.942C= MANE Select | ENSP00000498074.1:p.Gly314= | |
ENST00000650147.1:c.559C= | ||
ENST00000650437.1:c.433C= | ||
ENST00000360971.6:c.942C= | ENSP00000354238.2:p.Gly314= | |
ENST00000459624.1:n.12C= | ||
ENST00000513998.5:c.942C= | ENSP00000422424.1:p.Gly314= | |
NM_006208.2:c.942C= | NP_006199.2:p.Gly314= | |
NM_006208.3:c.942C= MANE Select | NP_006199.2:p.Gly314= |