ClinGen Allele Registry
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Canonical Allele Identifier:
CA32667229
Gene:
Linked Data
dbSNP Id:
rs76745622
gnomAD v2:
1-171621941-C-A
gnomAD v3:
1-171652801-C-A
gnomAD v4:
1-171652801-C-A
MyVariant Identifiers:
chr1:g.171621941C>A (hg19)
chr1:g.171652801C>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.171652801C>A , CM000663.2:g.171652801C>A
GRCh38
NC_000001.10:g.171621941C>A , CM000663.1:g.171621941C>A
GRCh37
NC_000001.9:g.169888564C>A
NCBI36
NG_008859.1:g.4833G>T
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