Canonical Allele Identifier: CA200491742
Gene:

Linked Data

dbSNP Id: rs535987343
gnomAD v3: 9-129576930-C-G
gnomAD v4: 9-129576930-C-G
MyVariant Identifiers: chr9:g.132339209C>G (hg19) chr9:g.129576930C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576930C>G , CM000671.2:g.129576930C>G GRCh38
NC_000009.11:g.132339209C>G , CM000671.1:g.132339209C>G GRCh37
NC_000009.10:g.131379030C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1332C>G
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Search 100 bp 3'