Canonical Allele Identifier: CA72865137
Gene: ITGA9 HGNC NCBI

Linked Data

dbSNP Id: rs569486615
gnomAD v2: 3-37603972-G-A
gnomAD v3: 3-37562481-G-A
gnomAD v4: 3-37562481-G-A
MyVariant Identifiers: chr3:g.37603972G>A (hg19) chr3:g.37562481G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562481G>A , CM000665.2:g.37562481G>A GRCh38
NC_000003.11:g.37603972G>A , CM000665.1:g.37603972G>A GRCh37
NC_000003.10:g.37578976G>A NCBI36
NG_016166.1:g.115160G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19896G>A MANE Select ENSP00000264741.5:n.1689+19896G>A
ENST00000264741.9:c.1689+19896G>A ENSP00000264741.5:n.1689+19896G>A
ENST00000422441.5:c.1689+19896G>A ENSP00000397258.1:n.1689+19896G>A
NM_002207.2:c.1689+19896G>A NP_002198.2:n.1689+19896G>A
NM_002207.3:c.1689+19896G>A MANE Select NP_002198.2:n.1689+19896G>A
Search 100 bp 5'
Search 100 bp 3'