Canonical Allele Identifier: CA290942711

Gene: ITGA2B

Linked Data

• dbSNP Id: rs899378886
• MyVariant Identifiers: chr17:g.42449706C>G (hg19) ; chr17:g.44372338C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44372338C>G , CM000679.2:g.44372338C>G	GRCh38
NC_000017.10:g.42449706C>G , CM000679.1:g.42449706C>G	GRCh37
NC_000017.9:g.39805232C>G	NCBI36
NG_008331.1:g.22168G>C , LRG_479:g.22168G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.*26G>C MANE Select	ENSP00000262407.5:n.*26G>C
ENST00000648408.1:c.2460G>C
ENST00000262407.5:c.*26G>C	ENSP00000262407.5:n.*26G>C
ENST00000587295.5:c.339G>C
ENST00000588098.1:c.123G>C
NM_000419.3:c.*26G>C , LRG_479t1:c.*26G>C	NP_000410.2:n.*26G>C
XM_011524749.1:c.*26G>C	XP_011523051.1:n.*26G>C
XM_011524750.1:c.*26G>C	XP_011523052.1:n.*26G>C
NM_000419.4:c.*26G>C	NP_000410.2:n.*26G>C
NM_000419.5:c.*26G>C MANE Select	NP_000410.2:n.*26G>C