Canonical Allele Identifier: CA399787913
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372415G>C , CM000679.2:g.44372415G>C GRCh38
NC_000017.10:g.42449783G>C , CM000679.1:g.42449783G>C GRCh37
NC_000017.9:g.39805309G>C NCBI36
NG_008331.1:g.22091C>G , LRG_479:g.22091C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3069C>G MANE Select ENSP00000262407.5:p.Phe1023Leu
ENST00000648408.1:c.2383C>G
ENST00000262407.5:c.3069C>G ENSP00000262407.5:p.Phe1023Leu
ENST00000587295.5:c.262C>G
ENST00000588098.1:c.46C>G
NM_000419.3:c.3069C>G , LRG_479t1:c.3069C>G NP_000410.2:p.Phe1023Leu
XM_011524749.1:c.2967C>G XP_011523051.1:p.Phe989Leu
XM_011524750.1:c.2952C>G XP_011523052.1:p.Phe984Leu
NM_000419.4:c.3069C>G NP_000410.2:p.Phe1023Leu
NM_000419.5:c.3069C>G MANE Select NP_000410.2:p.Phe1023Leu