Canonical Allele Identifier: CA262598192
Gene:

Linked Data

ClinVar Variation Id: 464899
ClinVar RCV Id: RCV001516352 RCV003222026 RCV003925647
dbSNP Id: rs34086577
gnomAD v2: 14-73602899-C-G
gnomAD v3: 14-73136191-C-G
gnomAD v4: 14-73136191-C-G
MyVariant Identifiers: chr14:g.73602899C>G (hg19) chr14:g.73136191C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73136191C>G , CM000676.2:g.73136191C>G GRCh38
NC_000014.8:g.73602899C>G , CM000676.1:g.73602899C>G GRCh37
NC_000014.7:g.72672652C>G NCBI36
NG_007386.2:g.4721C>G
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