Canonical Allele Identifier: CA2638216895

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44384209-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44384209G>T , CM000679.2:g.44384209G>T	GRCh38
NC_000017.10:g.42461577G>T , CM000679.1:g.42461577G>T	GRCh37
NC_000017.9:g.39817103G>T	NCBI36
NG_008331.1:g.10297C>A , LRG_479:g.10297C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262407.6:c.892-71C>A MANE Select	ENSP00000262407.5:n.892-71C>A
ENST00000648408.1:c.323-71C>A
ENST00000262407.5:c.892-71C>A	ENSP00000262407.5:n.892-71C>A
ENST00000589645.5:n.343-71C>A
ENST00000591990.5:n.437-71C>A
ENST00000592075.5:n.261-71C>A
ENST00000592226.5:n.132-71C>A
ENST00000592253.5:n.400-71C>A
NM_000419.3:c.892-71C>A , LRG_479t1:c.892-71C>A	NP_000410.2:n.892-71C>A
XM_011524749.1:c.892-71C>A	XP_011523051.1:n.892-71C>A
XM_011524750.1:c.892-71C>A	XP_011523052.1:n.892-71C>A
NM_000419.4:c.892-71C>A	NP_000410.2:n.892-71C>A
NM_000419.5:c.892-71C>A MANE Select	NP_000410.2:n.892-71C>A