Canonical Allele Identifier: CA399801904
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379785G>C , CM000679.2:g.44379785G>C GRCh38
NC_000017.10:g.42457153G>C , CM000679.1:g.42457153G>C GRCh37
NC_000017.9:g.39812679G>C NCBI36
NG_008331.1:g.14721C>G , LRG_479:g.14721C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1782C>G MANE Select ENSP00000262407.5:p.Ser594Arg
ENST00000648408.1:c.1213C>G
ENST00000262407.5:c.1782C>G ENSP00000262407.5:p.Ser594Arg
ENST00000592462.5:n.577C>G
NM_000419.3:c.1782C>G , LRG_479t1:c.1782C>G NP_000410.2:p.Ser594Arg
XM_011524749.1:c.1782C>G XP_011523051.1:p.Ser594Arg
XM_011524750.1:c.1782C>G XP_011523052.1:p.Ser594Arg
NM_000419.4:c.1782C>G NP_000410.2:p.Ser594Arg
NM_000419.5:c.1782C>G MANE Select NP_000410.2:p.Ser594Arg