Canonical Allele Identifier: CA399787693
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372381C>T , CM000679.2:g.44372381C>T GRCh38
NC_000017.10:g.42449749C>T , CM000679.1:g.42449749C>T GRCh37
NC_000017.9:g.39805275C>T NCBI36
NG_008331.1:g.22125G>A , LRG_479:g.22125G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3103G>A MANE Select ENSP00000262407.5:p.Asp1035Asn
ENST00000648408.1:c.2417G>A
ENST00000262407.5:c.3103G>A ENSP00000262407.5:p.Asp1035Asn
ENST00000587295.5:c.296G>A
ENST00000588098.1:c.80G>A
NM_000419.3:c.3103G>A , LRG_479t1:c.3103G>A NP_000410.2:p.Asp1035Asn
XM_011524749.1:c.3001G>A XP_011523051.1:p.Asp1001Asn
XM_011524750.1:c.2986G>A XP_011523052.1:p.Asp996Asn
NM_000419.4:c.3103G>A NP_000410.2:p.Asp1035Asn
NM_000419.5:c.3103G>A MANE Select NP_000410.2:p.Asp1035Asn