HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58930821A>T , CM000679.2:g.58930821A>T | GRCh38 |
NC_000017.10:g.57008182A>T , CM000679.1:g.57008182A>T | GRCh37 |
NC_000017.9:g.54362964A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308249.4:c.465-24828A>T MANE Select | ENSP00000312411.2:n.465-24828A>T | |
ENST00000308249.3:c.465-24828A>T | ENSP00000312411.2:n.465-24828A>T | |
NM_014906.4:c.465-24828A>T | NP_055721.3:n.465-24828A>T | |
NR_048561.1:n.594-24828A>T | ||
XM_011524534.1:c.-47-24828A>T | XP_011522836.1:n.-47-24828A>T | |
XM_024450657.1:c.-253-24828A>T | XP_024306425.1:n.-253-24828A>T | |
NM_014906.5:c.465-24828A>T MANE Select | NP_055721.3:n.465-24828A>T |