Canonical Allele Identifier: CA399792813

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44375605-C-T
• MyVariant Identifiers: chr17:g.42452973C>T (hg19) ; chr17:g.44375605C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44375605C>T , CM000679.2:g.44375605C>T	GRCh38
NC_000017.10:g.42452973C>T , CM000679.1:g.42452973C>T	GRCh37
NC_000017.9:g.39808499C>T	NCBI36
NG_008331.1:g.18901G>A , LRG_479:g.18901G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.2713G>A MANE Select	ENSP00000262407.5:p.Asp905Asn
ENST00000648408.1:c.2144G>A
ENST00000262407.5:c.2713G>A	ENSP00000262407.5:p.Asp905Asn
ENST00000587295.5:c.253+228G>A
ENST00000592462.5:n.1508G>A
NM_000419.3:c.2713G>A , LRG_479t1:c.2713G>A	NP_000410.2:p.Asp905Asn
XM_011524749.1:c.2713G>A	XP_011523051.1:p.Asp905Asn
XM_011524750.1:c.2713G>A	XP_011523052.1:p.Asp905Asn
NM_000419.4:c.2713G>A	NP_000410.2:p.Asp905Asn
NM_000419.5:c.2713G>A MANE Select	NP_000410.2:p.Asp905Asn