Canonical Allele Identifier: CA399803700
Gene: ITGA2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44380996G>T , CM000679.2:g.44380996G>T GRCh38
NC_000017.10:g.42458364G>T , CM000679.1:g.42458364G>T GRCh37
NC_000017.9:g.39813890G>T NCBI36
NG_008331.1:g.13510C>A , LRG_479:g.13510C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262407.6:c.1276C>A MANE Select ENSP00000262407.5:p.Gln426Lys
ENST00000648408.1:c.707C>A
ENST00000262407.5:c.1276C>A ENSP00000262407.5:p.Gln426Lys
ENST00000592226.5:n.516C>A
ENST00000592462.5:n.71C>A
NM_000419.3:c.1276C>A , LRG_479t1:c.1276C>A NP_000410.2:p.Gln426Lys
XM_011524749.1:c.1276C>A XP_011523051.1:p.Gln426Lys
XM_011524750.1:c.1276C>A XP_011523052.1:p.Gln426Lys
NM_000419.4:c.1276C>A NP_000410.2:p.Gln426Lys
NM_000419.5:c.1276C>A MANE Select NP_000410.2:p.Gln426Lys