Canonical Allele Identifier: CA2261365164

Gene: ITGA2B

Linked Data

• dbSNP Id: rs1304362291

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374278C>G , CM000679.2:g.44374278C>G	GRCh38
NC_000017.10:g.42451646C>G , CM000679.1:g.42451646C>G	GRCh37
NC_000017.9:g.39807172C>G	NCBI36
NG_008331.1:g.20228G>C , LRG_479:g.20228G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.3060+76G>C MANE Select	ENSP00000262407.5:n.3060+76G>C
ENST00000648408.1:c.2374+381G>C
ENST00000262407.5:c.3060+76G>C	ENSP00000262407.5:n.3060+76G>C
ENST00000587295.5:c.253+1555G>C
ENST00000588098.1:c.37+381G>C
ENST00000592462.5:n.2835G>C
NM_000419.3:c.3060+76G>C , LRG_479t1:c.3060+76G>C	NP_000410.2:n.3060+76G>C
XM_011524749.1:c.2958+76G>C	XP_011523051.1:n.2958+76G>C
XM_011524750.1:c.2943+381G>C	XP_011523052.1:n.2943+381G>C
NM_000419.4:c.3060+76G>C	NP_000410.2:n.3060+76G>C
NM_000419.5:c.3060+76G>C MANE Select	NP_000410.2:n.3060+76G>C