Canonical Allele Identifier: CA399801935
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379800G>T , CM000679.2:g.44379800G>T GRCh38
NC_000017.10:g.42457168G>T , CM000679.1:g.42457168G>T GRCh37
NC_000017.9:g.39812694G>T NCBI36
NG_008331.1:g.14706C>A , LRG_479:g.14706C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1767C>A MANE Select ENSP00000262407.5:p.Phe589Leu
ENST00000648408.1:c.1198C>A
ENST00000262407.5:c.1767C>A ENSP00000262407.5:p.Phe589Leu
ENST00000592462.5:n.562C>A
NM_000419.3:c.1767C>A , LRG_479t1:c.1767C>A NP_000410.2:p.Phe589Leu
XM_011524749.1:c.1767C>A XP_011523051.1:p.Phe589Leu
XM_011524750.1:c.1767C>A XP_011523052.1:p.Phe589Leu
NM_000419.4:c.1767C>A NP_000410.2:p.Phe589Leu
NM_000419.5:c.1767C>A MANE Select NP_000410.2:p.Phe589Leu