Canonical Allele Identifier: CA72865114
Gene: ITGA9 HGNC NCBI

Linked Data

dbSNP Id: rs945603834
gnomAD v3: 3-37562417-C-G
gnomAD v4: 3-37562417-C-G
MyVariant Identifiers: chr3:g.37603908C>G (hg19) chr3:g.37562417C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562417C>G , CM000665.2:g.37562417C>G GRCh38
NC_000003.11:g.37603908C>G , CM000665.1:g.37603908C>G GRCh37
NC_000003.10:g.37578912C>G NCBI36
NG_016166.1:g.115096C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19832C>G MANE Select ENSP00000264741.5:n.1689+19832C>G
ENST00000264741.9:c.1689+19832C>G ENSP00000264741.5:n.1689+19832C>G
ENST00000422441.5:c.1689+19832C>G ENSP00000397258.1:n.1689+19832C>G
NM_002207.2:c.1689+19832C>G NP_002198.2:n.1689+19832C>G
NM_002207.3:c.1689+19832C>G MANE Select NP_002198.2:n.1689+19832C>G
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