Canonical Allele Identifier: CA500279266

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42461946C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384578C>G , CM000679.2:g.44384578C>G	GRCh38
NC_000017.10:g.42461946C>G , CM000679.1:g.42461946C>G	GRCh37
NC_000017.9:g.39817472C>G	NCBI36
NG_008331.1:g.9928G>C , LRG_479:g.9928G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.807G>C MANE Select	ENSP00000262407.5:p.Ser269=
ENST00000648408.1:c.238G>C
ENST00000262407.5:c.807G>C	ENSP00000262407.5:p.Ser269=
ENST00000589645.5:n.258G>C
ENST00000591990.5:n.169G>C
ENST00000592075.5:n.176G>C
ENST00000592226.5:n.47G>C
ENST00000592253.5:n.315G>C
ENST00000592944.1:n.489G>C
NM_000419.3:c.807G>C , LRG_479t1:c.807G>C	NP_000410.2:p.Ser269=
XM_011524749.1:c.807G>C	XP_011523051.1:p.Ser269=
XM_011524750.1:c.807G>C	XP_011523052.1:p.Ser269=
NM_000419.4:c.807G>C	NP_000410.2:p.Ser269=
NM_000419.5:c.807G>C MANE Select	NP_000410.2:p.Ser269=