Canonical Allele Identifier: CA399798929

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42455088T>C (hg19) ; chr17:g.44377720T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44377720T>C , CM000679.2:g.44377720T>C	GRCh38
NC_000017.10:g.42455088T>C , CM000679.1:g.42455088T>C	GRCh37
NC_000017.9:g.39810614T>C	NCBI36
NG_008331.1:g.16786A>G , LRG_479:g.16786A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2165A>G MANE Select	ENSP00000262407.5:p.Asn722Ser
ENST00000648408.1:c.1596A>G
ENST00000262407.5:c.2165A>G	ENSP00000262407.5:p.Asn722Ser
ENST00000592462.5:n.960A>G
NM_000419.3:c.2165A>G , LRG_479t1:c.2165A>G	NP_000410.2:p.Asn722Ser
XM_011524749.1:c.2165A>G	XP_011523051.1:p.Asn722Ser
XM_011524750.1:c.2165A>G	XP_011523052.1:p.Asn722Ser
NM_000419.4:c.2165A>G	NP_000410.2:p.Asn722Ser
NM_000419.5:c.2165A>G MANE Select	NP_000410.2:p.Asn722Ser