Canonical Allele Identifier: CA399805992

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42463059T>A (hg19) ; chr17:g.44385691T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385691T>A , CM000679.2:g.44385691T>A	GRCh38
NC_000017.10:g.42463059T>A , CM000679.1:g.42463059T>A	GRCh37
NC_000017.9:g.39818585T>A	NCBI36
NG_008331.1:g.8815A>T , LRG_479:g.8815A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.434A>T MANE Select	ENSP00000262407.5:p.Asn145Ile
ENST00000262407.5:c.434A>T	ENSP00000262407.5:p.Asn145Ile
ENST00000592944.1:n.119A>T
NM_000419.3:c.434A>T , LRG_479t1:c.434A>T	NP_000410.2:p.Asn145Ile
XM_011524749.1:c.434A>T	XP_011523051.1:p.Asn145Ile
XM_011524750.1:c.434A>T	XP_011523052.1:p.Asn145Ile
NM_000419.4:c.434A>T	NP_000410.2:p.Asn145Ile
NM_000419.5:c.434A>T MANE Select	NP_000410.2:p.Asn145Ile