Canonical Allele Identifier: CA626121677
Gene: ITGA2B HGNC NCBI

Linked Data

dbSNP Id: rs201295296

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379644A>C , CM000679.2:g.44379644A>C GRCh38
NC_000017.10:g.42457012A>C , CM000679.1:g.42457012A>C GRCh37
NC_000017.9:g.39812538A>C NCBI36
NG_008331.1:g.14862T>G , LRG_479:g.14862T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1878+45T>G MANE Select ENSP00000262407.5:n.1878+45T>G
ENST00000648408.1:c.1309+45T>G
ENST00000262407.5:c.1878+45T>G ENSP00000262407.5:n.1878+45T>G
ENST00000592462.5:n.673+45T>G
NM_000419.3:c.1878+45T>G , LRG_479t1:c.1878+45T>G NP_000410.2:n.1878+45T>G
XM_011524749.1:c.1878+45T>G XP_011523051.1:n.1878+45T>G
XM_011524750.1:c.1878+45T>G XP_011523052.1:n.1878+45T>G
NM_000419.4:c.1878+45T>G NP_000410.2:n.1878+45T>G
NM_000419.5:c.1878+45T>G MANE Select NP_000410.2:n.1878+45T>G