HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31622889C>A , CM000668.2:g.31622889C>A | GRCh38 |
NC_000006.11:g.31590666C>A , CM000668.1:g.31590666C>A | GRCh37 |
NC_000006.10:g.31698645C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376033.3:c.100C>A MANE Select | ENSP00000365201.2:p.Gln34Lys | |
ENST00000376007.8:c.100C>A | ENSP00000365175.4:p.Gln34Lys | |
ENST00000376033.2:c.100C>A | ENSP00000365201.2:p.Gln34Lys | |
ENST00000469577.5:n.136-1372C>A | ||
NM_004638.3:c.100C>A | NP_004629.3:p.Gln34Lys | |
NM_080686.2:c.100C>A | NP_542417.2:p.Gln34Lys | |
XM_011514890.1:c.100C>A | XP_011513192.1:p.Gln34Lys | |
XM_017011274.1:c.100C>A | XP_016866763.1:p.Gln34Lys | |
NM_004638.4:c.100C>A MANE Select | NP_004629.3:p.Gln34Lys | |
NM_080686.3:c.100C>A | NP_542417.2:p.Gln34Lys |