Canonical Allele Identifier: CA2261367805
Gene: ITGA2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379791C= , CM000679.2:g.44379791C= GRCh38
NC_000017.10:g.42457159C= , CM000679.1:g.42457159C= GRCh37
NC_000017.9:g.39812685C= NCBI36
NG_008331.1:g.14715G= , LRG_479:g.14715G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1776G= MANE Select ENSP00000262407.5:p.Lys592=
ENST00000648408.1:c.1207G=
ENST00000262407.5:c.1776G= ENSP00000262407.5:p.Lys592=
ENST00000592462.5:n.571G=
NM_000419.3:c.1776G= , LRG_479t1:c.1776G= NP_000410.2:p.Lys592=
XM_011524749.1:c.1776G= XP_011523051.1:p.Lys592=
XM_011524750.1:c.1776G= XP_011523052.1:p.Lys592=
NM_000419.4:c.1776G= NP_000410.2:p.Lys592=
NM_000419.5:c.1776G= MANE Select NP_000410.2:p.Lys592=