Canonical Allele Identifier: CA500271602
Gene: ITGA2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42457063C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379695C>T , CM000679.2:g.44379695C>T GRCh38
NC_000017.10:g.42457063C>T , CM000679.1:g.42457063C>T GRCh37
NC_000017.9:g.39812589C>T NCBI36
NG_008331.1:g.14811G>A , LRG_479:g.14811G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1872G>A MANE Select ENSP00000262407.5:p.Gln624=
ENST00000648408.1:c.1303G>A
ENST00000262407.5:c.1872G>A ENSP00000262407.5:p.Gln624=
ENST00000592462.5:n.667G>A
NM_000419.3:c.1872G>A , LRG_479t1:c.1872G>A NP_000410.2:p.Gln624=
XM_011524749.1:c.1872G>A XP_011523051.1:p.Gln624=
XM_011524750.1:c.1872G>A XP_011523052.1:p.Gln624=
NM_000419.4:c.1872G>A NP_000410.2:p.Gln624=
NM_000419.5:c.1872G>A MANE Select NP_000410.2:p.Gln624=