Canonical Allele Identifier: CA399801951
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379804T>C , CM000679.2:g.44379804T>C GRCh38
NC_000017.10:g.42457172T>C , CM000679.1:g.42457172T>C GRCh37
NC_000017.9:g.39812698T>C NCBI36
NG_008331.1:g.14702A>G , LRG_479:g.14702A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1763A>G MANE Select ENSP00000262407.5:p.Asp588Gly
ENST00000648408.1:c.1194A>G
ENST00000262407.5:c.1763A>G ENSP00000262407.5:p.Asp588Gly
ENST00000592462.5:n.558A>G
NM_000419.3:c.1763A>G , LRG_479t1:c.1763A>G NP_000410.2:p.Asp588Gly
XM_011524749.1:c.1763A>G XP_011523051.1:p.Asp588Gly
XM_011524750.1:c.1763A>G XP_011523052.1:p.Asp588Gly
NM_000419.4:c.1763A>G NP_000410.2:p.Asp588Gly
NM_000419.5:c.1763A>G MANE Select NP_000410.2:p.Asp588Gly