Canonical Allele Identifier: CA500271680
Gene: ITGA2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42457078T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379710T>C , CM000679.2:g.44379710T>C GRCh38
NC_000017.10:g.42457078T>C , CM000679.1:g.42457078T>C GRCh37
NC_000017.9:g.39812604T>C NCBI36
NG_008331.1:g.14796A>G , LRG_479:g.14796A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1857A>G MANE Select ENSP00000262407.5:p.Gly619=
ENST00000648408.1:c.1288A>G
ENST00000262407.5:c.1857A>G ENSP00000262407.5:p.Gly619=
ENST00000592462.5:n.652A>G
NM_000419.3:c.1857A>G , LRG_479t1:c.1857A>G NP_000410.2:p.Gly619=
XM_011524749.1:c.1857A>G XP_011523051.1:p.Gly619=
XM_011524750.1:c.1857A>G XP_011523052.1:p.Gly619=
NM_000419.4:c.1857A>G NP_000410.2:p.Gly619=
NM_000419.5:c.1857A>G MANE Select NP_000410.2:p.Gly619=