Canonical Allele Identifier: CA399791788
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375035G>C , CM000679.2:g.44375035G>C GRCh38
NC_000017.10:g.42452403G>C , CM000679.1:g.42452403G>C GRCh37
NC_000017.9:g.39807929G>C NCBI36
NG_008331.1:g.19471C>G , LRG_479:g.19471C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.2804C>G MANE Select ENSP00000262407.5:p.Thr935Arg
ENST00000648408.1:c.2235C>G
ENST00000262407.5:c.2804C>G ENSP00000262407.5:p.Thr935Arg
ENST00000587295.5:c.253+798C>G
ENST00000592462.5:n.2078C>G
NM_000419.3:c.2804C>G , LRG_479t1:c.2804C>G NP_000410.2:p.Thr935Arg
XM_011524749.1:c.2804C>G XP_011523051.1:p.Thr935Arg
XM_011524750.1:c.2804C>G XP_011523052.1:p.Thr935Arg
NM_000419.4:c.2804C>G NP_000410.2:p.Thr935Arg
NM_000419.5:c.2804C>G MANE Select NP_000410.2:p.Thr935Arg