Canonical Allele Identifier: CA8602535
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs756678813

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44374693A>G , CM000679.2:g.44374693A>G GRCh38
NC_000017.10:g.42452061A>G , CM000679.1:g.42452061A>G GRCh37
NC_000017.9:g.39807587A>G NCBI36
NG_008331.1:g.19813T>C , LRG_479:g.19813T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2909T>C MANE Select ENSP00000262407.5:p.Val970Ala
ENST00000648408.1:c.2340T>C
ENST00000262407.5:c.2909T>C ENSP00000262407.5:p.Val970Ala
ENST00000587295.5:c.253+1140T>C
ENST00000588098.1:c.3T>C
ENST00000592462.5:n.2420T>C
NM_000419.3:c.2909T>C , LRG_479t1:c.2909T>C NP_000410.2:p.Val970Ala
XM_011524749.1:c.2842-223T>C XP_011523051.1:n.2842-223T>C
XM_011524750.1:c.2909T>C XP_011523052.1:p.Val970Ala
NM_000419.4:c.2909T>C NP_000410.2:p.Val970Ala
NM_000419.5:c.2909T>C MANE Select NP_000410.2:p.Val970Ala