Canonical Allele Identifier: CA399787905
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372414A>C , CM000679.2:g.44372414A>C GRCh38
NC_000017.10:g.42449782A>C , CM000679.1:g.42449782A>C GRCh37
NC_000017.9:g.39805308A>C NCBI36
NG_008331.1:g.22092T>G , LRG_479:g.22092T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.3070T>G MANE Select ENSP00000262407.5:p.Phe1024Val
ENST00000648408.1:c.2384T>G
ENST00000262407.5:c.3070T>G ENSP00000262407.5:p.Phe1024Val
ENST00000587295.5:c.263T>G
ENST00000588098.1:c.47T>G
NM_000419.3:c.3070T>G , LRG_479t1:c.3070T>G NP_000410.2:p.Phe1024Val
XM_011524749.1:c.2968T>G XP_011523051.1:p.Phe990Val
XM_011524750.1:c.2953T>G XP_011523052.1:p.Phe985Val
NM_000419.4:c.3070T>G NP_000410.2:p.Phe1024Val
NM_000419.5:c.3070T>G MANE Select NP_000410.2:p.Phe1024Val