Canonical Allele Identifier: CA399787663
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44372377T>C , CM000679.2:g.44372377T>C GRCh38
NC_000017.10:g.42449745T>C , CM000679.1:g.42449745T>C GRCh37
NC_000017.9:g.39805271T>C NCBI36
NG_008331.1:g.22129A>G , LRG_479:g.22129A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.3107A>G MANE Select ENSP00000262407.5:p.Glu1036Gly
ENST00000648408.1:c.2421A>G
ENST00000262407.5:c.3107A>G ENSP00000262407.5:p.Glu1036Gly
ENST00000587295.5:c.300A>G
ENST00000588098.1:c.84A>G
NM_000419.3:c.3107A>G , LRG_479t1:c.3107A>G NP_000410.2:p.Glu1036Gly
XM_011524749.1:c.3005A>G XP_011523051.1:p.Glu1002Gly
XM_011524750.1:c.2990A>G XP_011523052.1:p.Glu997Gly
NM_000419.4:c.3107A>G NP_000410.2:p.Glu1036Gly
NM_000419.5:c.3107A>G MANE Select NP_000410.2:p.Glu1036Gly