Canonical Allele Identifier: CA399796689

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42453695C>A (hg19) ; chr17:g.44376327C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44376327C>A , CM000679.2:g.44376327C>A	GRCh38
NC_000017.10:g.42453695C>A , CM000679.1:g.42453695C>A	GRCh37
NC_000017.9:g.39809221C>A	NCBI36
NG_008331.1:g.18179G>T , LRG_479:g.18179G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2329G>T MANE Select	ENSP00000262407.5:p.Ala777Ser
ENST00000648408.1:c.1760G>T
ENST00000262407.5:c.2329G>T	ENSP00000262407.5:p.Ala777Ser
ENST00000592462.5:n.1124G>T
NM_000419.3:c.2329G>T , LRG_479t1:c.2329G>T	NP_000410.2:p.Ala777Ser
XM_011524749.1:c.2329G>T	XP_011523051.1:p.Ala777Ser
XM_011524750.1:c.2329G>T	XP_011523052.1:p.Ala777Ser
NM_000419.4:c.2329G>T	NP_000410.2:p.Ala777Ser
NM_000419.5:c.2329G>T MANE Select	NP_000410.2:p.Ala777Ser