Canonical Allele Identifier: CA906771219
Gene: ITGA9 HGNC NCBI

Linked Data

dbSNP Id: rs1007606959
gnomAD v3: 3-37562472-C-A
gnomAD v4: 3-37562472-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562472C>A , CM000665.2:g.37562472C>A GRCh38
NC_000003.11:g.37603963C>A , CM000665.1:g.37603963C>A GRCh37
NC_000003.10:g.37578967C>A NCBI36
NG_016166.1:g.115151C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19887C>A MANE Select ENSP00000264741.5:n.1689+19887C>A
ENST00000264741.9:c.1689+19887C>A ENSP00000264741.5:n.1689+19887C>A
ENST00000422441.5:c.1689+19887C>A ENSP00000397258.1:n.1689+19887C>A
NM_002207.2:c.1689+19887C>A NP_002198.2:n.1689+19887C>A
NM_002207.3:c.1689+19887C>A MANE Select NP_002198.2:n.1689+19887C>A