Canonical Allele Identifier: CA399801920
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379793T>A , CM000679.2:g.44379793T>A GRCh38
NC_000017.10:g.42457161T>A , CM000679.1:g.42457161T>A GRCh37
NC_000017.9:g.39812687T>A NCBI36
NG_008331.1:g.14713A>T , LRG_479:g.14713A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1774A>T MANE Select ENSP00000262407.5:p.Lys592Ter
ENST00000648408.1:c.1205A>T
ENST00000262407.5:c.1774A>T ENSP00000262407.5:p.Lys592Ter
ENST00000592462.5:n.569A>T
NM_000419.3:c.1774A>T , LRG_479t1:c.1774A>T NP_000410.2:p.Lys592Ter
XM_011524749.1:c.1774A>T XP_011523051.1:p.Lys592Ter
XM_011524750.1:c.1774A>T XP_011523052.1:p.Lys592Ter
NM_000419.4:c.1774A>T NP_000410.2:p.Lys592Ter
NM_000419.5:c.1774A>T MANE Select NP_000410.2:p.Lys592Ter