ClinGen Allele Registry
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Canonical Allele Identifier:
CA162913765
Gene:
Linked Data
dbSNP Id:
rs901507934
MyVariant Identifiers:
chr7:g.94954550T>G (hg19)
chr7:g.95325238T>G (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.95325238T>G , CM000669.2:g.95325238T>G
GRCh38
NC_000007.13:g.94954550T>G , CM000669.1:g.94954550T>G
GRCh37
NC_000007.12:g.94792486T>G
NCBI36
NG_008779.1:g.4335A>C
NG_008779.2:g.4469A>C
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