Canonical Allele Identifier: CA72865139

Gene: ITGA9

Linked Data

• dbSNP Id: rs933156404
• gnomAD v2: 3-37603973-A-G
• gnomAD v3: 3-37562482-A-G
• gnomAD v4: 3-37562482-A-G
• MyVariant Identifiers: chr3:g.37603973A>G (hg19) ; chr3:g.37562482A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.37562482A>G , CM000665.2:g.37562482A>G	GRCh38
NC_000003.11:g.37603973A>G , CM000665.1:g.37603973A>G	GRCh37
NC_000003.10:g.37578977A>G	NCBI36
NG_016166.1:g.115161A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264741.10:c.1689+19897A>G MANE Select	ENSP00000264741.5:n.1689+19897A>G
ENST00000264741.9:c.1689+19897A>G	ENSP00000264741.5:n.1689+19897A>G
ENST00000422441.5:c.1689+19897A>G	ENSP00000397258.1:n.1689+19897A>G
NM_002207.2:c.1689+19897A>G	NP_002198.2:n.1689+19897A>G
NM_002207.3:c.1689+19897A>G MANE Select	NP_002198.2:n.1689+19897A>G