Canonical Allele Identifier: CA8602447

Gene: ITGA2B

Linked Data

• dbSNP Id: rs541835140
• ExAC: 17:42449700 A / G
• gnomAD v2: 17-42449700-A-G
• gnomAD v3: 17-44372332-A-G
• gnomAD v4: 17-44372332-A-G
• MyVariant Identifiers: chr17:g.42449700A>G (hg19) ; chr17:g.44372332A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372332A>G , CM000679.2:g.44372332A>G	GRCh38
NC_000017.10:g.42449700A>G , CM000679.1:g.42449700A>G	GRCh37
NC_000017.9:g.39805226A>G	NCBI36
NG_008331.1:g.22174T>C , LRG_479:g.22174T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.*32T>C MANE Select	ENSP00000262407.5:n.*32T>C
ENST00000648408.1:c.2466T>C
ENST00000262407.5:c.*32T>C	ENSP00000262407.5:n.*32T>C
ENST00000587295.5:c.345T>C
ENST00000588098.1:c.129T>C
NM_000419.3:c.*32T>C , LRG_479t1:c.*32T>C	NP_000410.2:n.*32T>C
XM_011524749.1:c.*32T>C	XP_011523051.1:n.*32T>C
XM_011524750.1:c.*32T>C	XP_011523052.1:n.*32T>C
NM_000419.4:c.*32T>C	NP_000410.2:n.*32T>C
NM_000419.5:c.*32T>C MANE Select	NP_000410.2:n.*32T>C