Canonical Allele Identifier: CA858377624
Gene:

Linked Data

dbSNP Id: rs1359663896
gnomAD v3: 9-108092819-T-C
gnomAD v4: 9-108092819-T-C
MyVariant Identifiers: chr9:g.110855100T>C (hg19) chr9:g.108092819T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092819T>C , CM000671.2:g.108092819T>C GRCh38
NC_000009.11:g.110855100T>C , CM000671.1:g.110855100T>C GRCh37
NC_000009.10:g.109894921T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930239.1:n.461-39525A>G
XR_001746881.1:n.668-39525A>G
XR_001746882.1:n.668-39525A>G
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