Canonical Allele Identifier: CA399805362

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42462406T>C (hg19) ; chr17:g.44385038T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385038T>C , CM000679.2:g.44385038T>C	GRCh38
NC_000017.10:g.42462406T>C , CM000679.1:g.42462406T>C	GRCh37
NC_000017.9:g.39817932T>C	NCBI36
NG_008331.1:g.9468A>G , LRG_479:g.9468A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.709A>G MANE Select	ENSP00000262407.5:p.Ser237Gly
ENST00000648408.1:c.140A>G
ENST00000262407.5:c.709A>G	ENSP00000262407.5:p.Ser237Gly
ENST00000589645.5:n.160A>G
ENST00000591990.5:n.71A>G
ENST00000592075.5:n.78A>G
ENST00000592226.5:n.39+126A>G
ENST00000592253.5:n.217A>G
ENST00000592944.1:n.391A>G
NM_000419.3:c.709A>G , LRG_479t1:c.709A>G	NP_000410.2:p.Ser237Gly
XM_011524749.1:c.709A>G	XP_011523051.1:p.Ser237Gly
XM_011524750.1:c.709A>G	XP_011523052.1:p.Ser237Gly
NM_000419.4:c.709A>G	NP_000410.2:p.Ser237Gly
NM_000419.5:c.709A>G MANE Select	NP_000410.2:p.Ser237Gly