HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7526854C= , CM000681.2:g.7526854C= | GRCh38 |
NC_000019.9:g.7591740C= , CM000681.1:g.7591740C= | GRCh37 |
NC_000019.8:g.7497740C= | NCBI36 |
NG_015806.1:g.9245C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264079.11:c.499C= MANE Select | ENSP00000264079.5:p.Gln167= | |
ENST00000264079.10:c.499C= | ENSP00000264079.5:p.Gln167= | |
ENST00000394321.9:n.579C= | ||
ENST00000596008.1:n.461C= | ||
ENST00000598406.1:n.320C= | ||
ENST00000601003.1:c.499C= | ENSP00000469074.1:p.Gln167= | |
NM_020533.2:c.499C= | NP_065394.1:p.Gln167= | |
NM_020533.3:c.499C= MANE Select | NP_065394.1:p.Gln167= |