Canonical Allele Identifier: CA8603305

Gene: ITGA2B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384313C>G , CM000679.2:g.44384313C>G	GRCh38
NC_000017.10:g.42461681C>G , CM000679.1:g.42461681C>G	GRCh37
NC_000017.9:g.39817207C>G	NCBI36
NG_008331.1:g.10193G>C , LRG_479:g.10193G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000419.5:c.889G>C MANE Select	NP_000410.2:p.Ala297Pro
ENST00000262407.6:c.889G>C MANE Select	ENSP00000262407.5:p.Ala297Pro
NM_000419.3:c.889G>C , LRG_479t1:c.889G>C	NP_000410.2:p.Ala297Pro
NM_000419.4:c.889G>C	NP_000410.2:p.Ala297Pro
ENST00000262407.5:c.889G>C	ENSP00000262407.5:p.Ala297Pro
ENST00000589645.5:n.340G>C
ENST00000591990.5:n.434G>C
ENST00000592075.5:n.258G>C
ENST00000592226.5:n.129G>C
ENST00000592253.5:n.397G>C
ENST00000648408.1:c.320G>C
XM_011524749.1:c.889G>C	XP_011523051.1:p.Ala297Pro
XM_011524750.1:c.889G>C	XP_011523052.1:p.Ala297Pro