HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186199057C= , CM000666.2:g.186199057C= | GRCh38 |
NC_000004.11:g.187120211C= , CM000666.1:g.187120211C= | GRCh37 |
NC_000004.10:g.187357205C= | NCBI36 |
NG_007965.1:g.12538C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378802.5:c.775C= MANE Select | ENSP00000368079.4:p.Gln259= | |
ENST00000378802.4:c.775C= | ENSP00000368079.4:p.Gln259= | |
ENST00000507209.5:n.1616C= | ||
NM_207352.3:c.775C= | NP_997235.3:p.Gln259= | |
XM_005262935.2:c.775C= | XP_005262992.1:p.Gln259= | |
XM_006714184.2:c.379C= | XP_006714247.1:p.Gln127= | |
XM_005262935.4:c.775C= | XP_005262992.1:p.Gln259= | |
XM_017008037.1:c.379C= | XP_016863526.1:p.Gln127= | |
NM_207352.4:c.775C= MANE Select | NP_997235.3:p.Gln259= |