Canonical Allele Identifier: CA2740094967
Gene:

Linked Data

ClinVar Variation Id: 3036683
ClinVar RCV Id: RCV003921714
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11564614T>C , CM000670.2:g.11564614T>C GRCh38
NC_000008.10:g.11422123T>C , CM000670.1:g.11422123T>C GRCh37
NC_000008.9:g.11459532T>C NCBI36
NG_023543.1:g.75603T>C
NG_023543.2:g.75603T>C
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