Canonical Allele Identifier: CA188145887
Gene:

Linked Data

dbSNP Id: rs921848587
gnomAD v2: 9-1787683-C-A
gnomAD v3: 9-1787683-C-A
gnomAD v4: 9-1787683-C-A
MyVariant Identifiers: chr9:g.1787683C>A (hg19) chr9:g.1787683C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787683C>A , CM000671.2:g.1787683C>A GRCh38
NC_000009.11:g.1787683C>A , CM000671.1:g.1787683C>A GRCh37
NC_000009.10:g.1777683C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68771C>A
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