Canonical Allele Identifier: CA399801589
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379711C>A , CM000679.2:g.44379711C>A GRCh38
NC_000017.10:g.42457079C>A , CM000679.1:g.42457079C>A GRCh37
NC_000017.9:g.39812605C>A NCBI36
NG_008331.1:g.14795G>T , LRG_479:g.14795G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1856G>T MANE Select ENSP00000262407.5:p.Gly619Val
ENST00000648408.1:c.1287G>T
ENST00000262407.5:c.1856G>T ENSP00000262407.5:p.Gly619Val
ENST00000592462.5:n.651G>T
NM_000419.3:c.1856G>T , LRG_479t1:c.1856G>T NP_000410.2:p.Gly619Val
XM_011524749.1:c.1856G>T XP_011523051.1:p.Gly619Val
XM_011524750.1:c.1856G>T XP_011523052.1:p.Gly619Val
NM_000419.4:c.1856G>T NP_000410.2:p.Gly619Val
NM_000419.5:c.1856G>T MANE Select NP_000410.2:p.Gly619Val