ClinGen Allele Registry
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Canonical Allele Identifier:
CA764564983
Gene:
Linked Data
dbSNP Id:
rs1352727986
MyVariant Identifiers:
chr2:g.215674762A>G (hg19)
chr2:g.214810038A>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.214810038A>G , CM000664.2:g.214810038A>G
GRCh38
NC_000002.11:g.215674762A>G , CM000664.1:g.215674762A>G
GRCh37
NC_000002.10:g.215383007A>G
NCBI36
NG_012047.2:g.4667T>C
NG_012047.3:g.4674T>C
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