Canonical Allele Identifier: CA399791006
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374726G>A , CM000679.2:g.44374726G>A GRCh38
NC_000017.10:g.42452094G>A , CM000679.1:g.42452094G>A GRCh37
NC_000017.9:g.39807620G>A NCBI36
NG_008331.1:g.19780C>T , LRG_479:g.19780C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2876C>T MANE Select ENSP00000262407.5:p.Ala959Val
ENST00000648408.1:c.2307C>T
ENST00000262407.5:c.2876C>T ENSP00000262407.5:p.Ala959Val
ENST00000587295.5:c.253+1107C>T
ENST00000592462.5:n.2387C>T
NM_000419.3:c.2876C>T , LRG_479t1:c.2876C>T NP_000410.2:p.Ala959Val
XM_011524749.1:c.2842-256C>T XP_011523051.1:n.2842-256C>T
XM_011524750.1:c.2876C>T XP_011523052.1:p.Ala959Val
NM_000419.4:c.2876C>T NP_000410.2:p.Ala959Val
NM_000419.5:c.2876C>T MANE Select NP_000410.2:p.Ala959Val