Canonical Allele Identifier: CA500280130

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42462392G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385024G>C , CM000679.2:g.44385024G>C	GRCh38
NC_000017.10:g.42462392G>C , CM000679.1:g.42462392G>C	GRCh37
NC_000017.9:g.39817918G>C	NCBI36
NG_008331.1:g.9482C>G , LRG_479:g.9482C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.723C>G MANE Select	ENSP00000262407.5:p.Gly241=
ENST00000648408.1:c.154C>G
ENST00000262407.5:c.723C>G	ENSP00000262407.5:p.Gly241=
ENST00000589645.5:n.174C>G
ENST00000591990.5:n.85C>G
ENST00000592075.5:n.92C>G
ENST00000592226.5:n.39+140C>G
ENST00000592253.5:n.231C>G
ENST00000592944.1:n.405C>G
NM_000419.3:c.723C>G , LRG_479t1:c.723C>G	NP_000410.2:p.Gly241=
XM_011524749.1:c.723C>G	XP_011523051.1:p.Gly241=
XM_011524750.1:c.723C>G	XP_011523052.1:p.Gly241=
NM_000419.4:c.723C>G	NP_000410.2:p.Gly241=
NM_000419.5:c.723C>G MANE Select	NP_000410.2:p.Gly241=