Canonical Allele Identifier: CA399793691
Gene: ITGA2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.42453066T>C (hg19) chr17:g.44375698T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44375698T>C , CM000679.2:g.44375698T>C GRCh38
NC_000017.10:g.42453066T>C , CM000679.1:g.42453066T>C GRCh37
NC_000017.9:g.39808592T>C NCBI36
NG_008331.1:g.18808A>G , LRG_479:g.18808A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262407.6:c.2620A>G MANE Select ENSP00000262407.5:p.Ile874Val
ENST00000648408.1:c.2051A>G
ENST00000262407.5:c.2620A>G ENSP00000262407.5:p.Ile874Val
ENST00000587295.5:c.253+135A>G
ENST00000592462.5:n.1415A>G
NM_000419.3:c.2620A>G , LRG_479t1:c.2620A>G NP_000410.2:p.Ile874Val
XM_011524749.1:c.2620A>G XP_011523051.1:p.Ile874Val
XM_011524750.1:c.2620A>G XP_011523052.1:p.Ile874Val
NM_000419.4:c.2620A>G NP_000410.2:p.Ile874Val
NM_000419.5:c.2620A>G MANE Select NP_000410.2:p.Ile874Val
Search 100 bp 5'
Search 100 bp 3'