Canonical Allele Identifier: CA15137589
Gene:

Linked Data

ClinVar Variation Id: 1165021
ClinVar RCV Id: RCV001511738
dbSNP Id: rs763110
gnomAD v2: 1-172627498-C-T
gnomAD v3: 1-172658358-C-T
gnomAD v4: 1-172658358-C-T
MyVariant Identifiers: chr1:g.172627498C>T (hg19) chr1:g.172658358C>T (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172658358C>T , CM000663.2:g.172658358C>T GRCh38
NC_000001.10:g.172627498C>T , CM000663.1:g.172627498C>T GRCh37
NC_000001.9:g.170894121C>T NCBI36
NG_007269.1:g.4314C>T , LRG_58:g.4314C>T
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