Canonical Allele Identifier: CA542249065
Gene: ITGA9 HGNC NCBI

Linked Data

dbSNP Id: rs1447404045
gnomAD v2: 3-37603933-T-C
gnomAD v3: 3-37562442-T-C
gnomAD v4: 3-37562442-T-C
MyVariant Identifiers: chr3:g.37603933T>C (hg19) chr3:g.37562442T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.37562442T>C , CM000665.2:g.37562442T>C GRCh38
NC_000003.11:g.37603933T>C , CM000665.1:g.37603933T>C GRCh37
NC_000003.10:g.37578937T>C NCBI36
NG_016166.1:g.115121T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264741.10:c.1689+19857T>C MANE Select ENSP00000264741.5:n.1689+19857T>C
ENST00000264741.9:c.1689+19857T>C ENSP00000264741.5:n.1689+19857T>C
ENST00000422441.5:c.1689+19857T>C ENSP00000397258.1:n.1689+19857T>C
NM_002207.2:c.1689+19857T>C NP_002198.2:n.1689+19857T>C
NM_002207.3:c.1689+19857T>C MANE Select NP_002198.2:n.1689+19857T>C
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