Canonical Allele Identifier: CA399805329

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42462390A>T (hg19) ; chr17:g.44385022A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385022A>T , CM000679.2:g.44385022A>T	GRCh38
NC_000017.10:g.42462390A>T , CM000679.1:g.42462390A>T	GRCh37
NC_000017.9:g.39817916A>T	NCBI36
NG_008331.1:g.9484T>A , LRG_479:g.9484T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.725T>A MANE Select	ENSP00000262407.5:p.Ile242Asn
ENST00000648408.1:c.156T>A
ENST00000262407.5:c.725T>A	ENSP00000262407.5:p.Ile242Asn
ENST00000589645.5:n.176T>A
ENST00000591990.5:n.87T>A
ENST00000592075.5:n.94T>A
ENST00000592226.5:n.39+142T>A
ENST00000592253.5:n.233T>A
ENST00000592944.1:n.407T>A
NM_000419.3:c.725T>A , LRG_479t1:c.725T>A	NP_000410.2:p.Ile242Asn
XM_011524749.1:c.725T>A	XP_011523051.1:p.Ile242Asn
XM_011524750.1:c.725T>A	XP_011523052.1:p.Ile242Asn
NM_000419.4:c.725T>A	NP_000410.2:p.Ile242Asn
NM_000419.5:c.725T>A MANE Select	NP_000410.2:p.Ile242Asn