Canonical Allele Identifier: CA10691792
Gene:

Linked Data

ClinVar Variation Id: 1257032
ClinVar RCV Id: RCV001666182
dbSNP Id: rs34324629
gnomAD v2: 1-171622057-C-T
gnomAD v3: 1-171652917-C-T
gnomAD v4: 1-171652917-C-T
MyVariant Identifiers: chr1:g.171622057C>T (hg19) chr1:g.171652917C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652917C>T , CM000663.2:g.171652917C>T GRCh38
NC_000001.10:g.171622057C>T , CM000663.1:g.171622057C>T GRCh37
NC_000001.9:g.169888680C>T NCBI36
NG_008859.1:g.4717G>A
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