Canonical Allele Identifier: CA72865160
Gene: ITGA9 HGNC NCBI

Linked Data

dbSNP Id: rs765941495
MyVariant Identifiers: chr3:g.37604042G>A (hg19) chr3:g.37562551G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562551G>A , CM000665.2:g.37562551G>A GRCh38
NC_000003.11:g.37604042G>A , CM000665.1:g.37604042G>A GRCh37
NC_000003.10:g.37579046G>A NCBI36
NG_016166.1:g.115230G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19966G>A MANE Select ENSP00000264741.5:n.1689+19966G>A
ENST00000264741.9:c.1689+19966G>A ENSP00000264741.5:n.1689+19966G>A
ENST00000422441.5:c.1689+19966G>A ENSP00000397258.1:n.1689+19966G>A
NM_002207.2:c.1689+19966G>A NP_002198.2:n.1689+19966G>A
NM_002207.3:c.1689+19966G>A MANE Select NP_002198.2:n.1689+19966G>A
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