ClinGen Allele Registry
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Canonical Allele Identifier:
CA10691231
Gene:
Linked Data
dbSNP Id:
rs1800807
gnomAD v2:
1-169601435-C-G
gnomAD v3:
1-169632197-C-G
gnomAD v4:
1-169632197-C-G
MyVariant Identifiers:
chr1:g.169601435C>G (hg19)
chr1:g.169632197C>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.169632197C>G , CM000663.2:g.169632197C>G
GRCh38
NC_000001.10:g.169601435C>G , CM000663.1:g.169601435C>G
GRCh37
NC_000001.9:g.167868059C>G
NCBI36
NG_012125.1:g.2943G>C
NG_012125.2:g.2943G>C
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