Canonical Allele Identifier: CA2638217477

Gene: ITGA2B

Linked Data

• gnomAD v4: 17-44385120-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44385120C>T , CM000679.2:g.44385120C>T	GRCh38
NC_000017.10:g.42462488C>T , CM000679.1:g.42462488C>T	GRCh37
NC_000017.9:g.39818014C>T	NCBI36
NG_008331.1:g.9386G>A , LRG_479:g.9386G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262407.6:c.671-44G>A MANE Select	ENSP00000262407.5:n.671-44G>A
ENST00000648408.1:c.102-44G>A
ENST00000262407.5:c.671-44G>A	ENSP00000262407.5:n.671-44G>A
ENST00000589645.5:n.122-44G>A
ENST00000591990.5:n.33-44G>A
ENST00000592075.5:n.40-44G>A
ENST00000592226.5:n.39+44G>A
ENST00000592253.5:n.179-44G>A
ENST00000592944.1:n.353-44G>A
NM_000419.3:c.671-44G>A , LRG_479t1:c.671-44G>A	NP_000410.2:n.671-44G>A
XM_011524749.1:c.671-44G>A	XP_011523051.1:n.671-44G>A
XM_011524750.1:c.671-44G>A	XP_011523052.1:n.671-44G>A
NM_000419.4:c.671-44G>A	NP_000410.2:n.671-44G>A
NM_000419.5:c.671-44G>A MANE Select	NP_000410.2:n.671-44G>A