Canonical Allele Identifier: CA399787942
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372419C>G , CM000679.2:g.44372419C>G GRCh38
NC_000017.10:g.42449787C>G , CM000679.1:g.42449787C>G GRCh37
NC_000017.9:g.39805313C>G NCBI36
NG_008331.1:g.22087G>C , LRG_479:g.22087G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3065G>C MANE Select ENSP00000262407.5:p.Gly1022Ala
ENST00000648408.1:c.2379G>C
ENST00000262407.5:c.3065G>C ENSP00000262407.5:p.Gly1022Ala
ENST00000587295.5:c.258G>C
ENST00000588098.1:c.42G>C
NM_000419.3:c.3065G>C , LRG_479t1:c.3065G>C NP_000410.2:p.Gly1022Ala
XM_011524749.1:c.2963G>C XP_011523051.1:p.Gly988Ala
XM_011524750.1:c.2948G>C XP_011523052.1:p.Gly983Ala
NM_000419.4:c.3065G>C NP_000410.2:p.Gly1022Ala
NM_000419.5:c.3065G>C MANE Select NP_000410.2:p.Gly1022Ala