ClinGen Allele Registry
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Canonical Allele Identifier:
CA31677518
Gene:
Linked Data
dbSNP Id:
rs976563537
MyVariant Identifiers:
chr1:g.161184549T>C (hg19)
chr1:g.161214759T>C (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.161214759T>C , CM000663.2:g.161214759T>C
GRCh38
NC_000001.10:g.161184549T>C , CM000663.1:g.161184549T>C
GRCh37
NC_000001.9:g.159451173T>C
NCBI36
NG_013352.1:g.20445T>C
NG_029043.1:g.4463T>C
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