Canonical Allele Identifier: CA399801523
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379697G>T , CM000679.2:g.44379697G>T GRCh38
NC_000017.10:g.42457065G>T , CM000679.1:g.42457065G>T GRCh37
NC_000017.9:g.39812591G>T NCBI36
NG_008331.1:g.14809C>A , LRG_479:g.14809C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1870C>A MANE Select ENSP00000262407.5:p.Gln624Lys
ENST00000648408.1:c.1301C>A
ENST00000262407.5:c.1870C>A ENSP00000262407.5:p.Gln624Lys
ENST00000592462.5:n.665C>A
NM_000419.3:c.1870C>A , LRG_479t1:c.1870C>A NP_000410.2:p.Gln624Lys
XM_011524749.1:c.1870C>A XP_011523051.1:p.Gln624Lys
XM_011524750.1:c.1870C>A XP_011523052.1:p.Gln624Lys
NM_000419.4:c.1870C>A NP_000410.2:p.Gln624Lys
NM_000419.5:c.1870C>A MANE Select NP_000410.2:p.Gln624Lys