Canonical Allele Identifier: CA399805122

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42461941G>A (hg19) ; chr17:g.44384573G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384573G>A , CM000679.2:g.44384573G>A	GRCh38
NC_000017.10:g.42461941G>A , CM000679.1:g.42461941G>A	GRCh37
NC_000017.9:g.39817467G>A	NCBI36
NG_008331.1:g.9933C>T , LRG_479:g.9933C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.812C>T MANE Select	ENSP00000262407.5:p.Ala271Val
ENST00000648408.1:c.243C>T
ENST00000262407.5:c.812C>T	ENSP00000262407.5:p.Ala271Val
ENST00000589645.5:n.263C>T
ENST00000591990.5:n.174C>T
ENST00000592075.5:n.181C>T
ENST00000592226.5:n.52C>T
ENST00000592253.5:n.320C>T
ENST00000592944.1:n.494C>T
NM_000419.3:c.812C>T , LRG_479t1:c.812C>T	NP_000410.2:p.Ala271Val
XM_011524749.1:c.812C>T	XP_011523051.1:p.Ala271Val
XM_011524750.1:c.812C>T	XP_011523052.1:p.Ala271Val
NM_000419.4:c.812C>T	NP_000410.2:p.Ala271Val
NM_000419.5:c.812C>T MANE Select	NP_000410.2:p.Ala271Val