Canonical Allele Identifier: CA399790435

Gene: ITGA2B

Linked Data

• MyVariant Identifiers: chr17:g.42452032C>G (hg19) ; chr17:g.44374664C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374664C>G , CM000679.2:g.44374664C>G	GRCh38
NC_000017.10:g.42452032C>G , CM000679.1:g.42452032C>G	GRCh37
NC_000017.9:g.39807558C>G	NCBI36
NG_008331.1:g.19842G>C , LRG_479:g.19842G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2938G>C MANE Select	ENSP00000262407.5:p.Ala980Pro
ENST00000648408.1:c.2369G>C
ENST00000262407.5:c.2938G>C	ENSP00000262407.5:p.Ala980Pro
ENST00000587295.5:c.253+1169G>C
ENST00000588098.1:c.32G>C
ENST00000592462.5:n.2449G>C
NM_000419.3:c.2938G>C , LRG_479t1:c.2938G>C	NP_000410.2:p.Ala980Pro
XM_011524749.1:c.2842-194G>C	XP_011523051.1:n.2842-194G>C
XM_011524750.1:c.2938G>C	XP_011523052.1:p.Ala980Pro
NM_000419.4:c.2938G>C	NP_000410.2:p.Ala980Pro
NM_000419.5:c.2938G>C MANE Select	NP_000410.2:p.Ala980Pro