Canonical Allele Identifier: CA293095
Gene:

Linked Data

ClinVar Variation Id: 138921
ClinVar RCV Id: RCV000641015 RCV001274360
dbSNP Id: rs12551232
gnomAD v2: 9-35658070-T-C
gnomAD v3: 9-35658073-T-C
gnomAD v4: 9-35658073-T-C
MyVariant Identifiers: chr9:g.35658070T>C (hg19) chr9:g.35658073T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658073T>C , CM000671.2:g.35658073T>C GRCh38
NC_000009.11:g.35658070T>C , CM000671.1:g.35658070T>C GRCh37
NC_000009.10:g.35648070T>C NCBI36
NG_017041.1:g.4946A>G , LRG_163:g.4946A>G
NG_033120.1:g.4784T>C
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