Canonical Allele Identifier: CA772288652
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs1317393821

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379666G>C , CM000679.2:g.44379666G>C GRCh38
NC_000017.10:g.42457034G>C , CM000679.1:g.42457034G>C GRCh37
NC_000017.9:g.39812560G>C NCBI36
NG_008331.1:g.14840C>G , LRG_479:g.14840C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1878+23C>G MANE Select ENSP00000262407.5:n.1878+23C>G
ENST00000648408.1:c.1309+23C>G
ENST00000262407.5:c.1878+23C>G ENSP00000262407.5:n.1878+23C>G
ENST00000592462.5:n.673+23C>G
NM_000419.3:c.1878+23C>G , LRG_479t1:c.1878+23C>G NP_000410.2:n.1878+23C>G
XM_011524749.1:c.1878+23C>G XP_011523051.1:n.1878+23C>G
XM_011524750.1:c.1878+23C>G XP_011523052.1:n.1878+23C>G
NM_000419.4:c.1878+23C>G NP_000410.2:n.1878+23C>G
NM_000419.5:c.1878+23C>G MANE Select NP_000410.2:n.1878+23C>G