Canonical Allele Identifier: CA290946358

Gene: ITGA2B

Linked Data

• dbSNP Id: rs982046016
• gnomAD v4: 17-44374845-AAGC-A
• MyVariant Identifiers: chr17:g.42452214_42452216del (hg19) ; chr17:g.44374846_44374848del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44374846_44374848del , CM000679.2:g.44374846_44374848del	GRCh38
NC_000017.10:g.42452214_42452216del , CM000679.1:g.42452214_42452216del	GRCh37
NC_000017.9:g.39807740_39807742del	NCBI36
NG_008331.1:g.19658_19660del , LRG_479:g.19658_19660del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.2842-88_2842-86del MANE Select	ENSP00000262407.5:n.2842-88_2842-86del
ENST00000648408.1:c.2273-88_2273-86del
ENST00000262407.5:c.2842-88_2842-86del	ENSP00000262407.5:n.2842-88_2842-86del
ENST00000587295.5:c.253+985_253+987del
ENST00000592462.5:n.2265_2267del
NM_000419.3:c.2842-88_2842-86del , LRG_479t1:c.2842-88_2842-86del	NP_000410.2:n.2842-88_2842-86del
XM_011524749.1:c.2841+150_2841+152del	XP_011523051.1:n.2841+150_2841+152del
XM_011524750.1:c.2842-88_2842-86del	XP_011523052.1:n.2842-88_2842-86del
NM_000419.4:c.2842-88_2842-86del	NP_000410.2:n.2842-88_2842-86del
NM_000419.5:c.2842-88_2842-86del MANE Select	NP_000410.2:n.2842-88_2842-86del