Canonical Allele Identifier: CA2261365491

Gene: ITGA2B

Linked Data

• dbSNP Id: rs2048526580
• gnomAD v4: 17-44374949-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374949T>C , CM000679.2:g.44374949T>C	GRCh38
NC_000017.10:g.42452317T>C , CM000679.1:g.42452317T>C	GRCh37
NC_000017.9:g.39807843T>C	NCBI36
NG_008331.1:g.19557A>G , LRG_479:g.19557A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2841+49A>G MANE Select	ENSP00000262407.5:n.2841+49A>G
ENST00000648408.1:c.2272+49A>G
ENST00000262407.5:c.2841+49A>G	ENSP00000262407.5:n.2841+49A>G
ENST00000587295.5:c.253+884A>G
ENST00000592462.5:n.2164A>G
NM_000419.3:c.2841+49A>G , LRG_479t1:c.2841+49A>G	NP_000410.2:n.2841+49A>G
XM_011524749.1:c.2841+49A>G	XP_011523051.1:n.2841+49A>G
XM_011524750.1:c.2841+49A>G	XP_011523052.1:n.2841+49A>G
NM_000419.4:c.2841+49A>G	NP_000410.2:n.2841+49A>G
NM_000419.5:c.2841+49A>G MANE Select	NP_000410.2:n.2841+49A>G