Canonical Allele Identifier: CA399801477
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379690T>C , CM000679.2:g.44379690T>C GRCh38
NC_000017.10:g.42457058T>C , CM000679.1:g.42457058T>C GRCh37
NC_000017.9:g.39812584T>C NCBI36
NG_008331.1:g.14816A>G , LRG_479:g.14816A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1877A>G MANE Select ENSP00000262407.5:p.Gln626Arg
ENST00000648408.1:c.1308A>G
ENST00000262407.5:c.1877A>G ENSP00000262407.5:p.Gln626Arg
ENST00000592462.5:n.672A>G
NM_000419.3:c.1877A>G , LRG_479t1:c.1877A>G NP_000410.2:p.Gln626Arg
XM_011524749.1:c.1877A>G XP_011523051.1:p.Gln626Arg
XM_011524750.1:c.1877A>G XP_011523052.1:p.Gln626Arg
NM_000419.4:c.1877A>G NP_000410.2:p.Gln626Arg
NM_000419.5:c.1877A>G MANE Select NP_000410.2:p.Gln626Arg