Canonical Allele Identifier: CA399801591
Gene: ITGA2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42457079C>G (hg19) chr17:g.44379711C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44379711C>G , CM000679.2:g.44379711C>G GRCh38
NC_000017.10:g.42457079C>G , CM000679.1:g.42457079C>G GRCh37
NC_000017.9:g.39812605C>G NCBI36
NG_008331.1:g.14795G>C , LRG_479:g.14795G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.1856G>C MANE Select ENSP00000262407.5:p.Gly619Ala
ENST00000648408.1:c.1287G>C
ENST00000262407.5:c.1856G>C ENSP00000262407.5:p.Gly619Ala
ENST00000592462.5:n.651G>C
NM_000419.3:c.1856G>C , LRG_479t1:c.1856G>C NP_000410.2:p.Gly619Ala
XM_011524749.1:c.1856G>C XP_011523051.1:p.Gly619Ala
XM_011524750.1:c.1856G>C XP_011523052.1:p.Gly619Ala
NM_000419.4:c.1856G>C NP_000410.2:p.Gly619Ala
NM_000419.5:c.1856G>C MANE Select NP_000410.2:p.Gly619Ala
Search 100 bp 5'
Search 100 bp 3'