ClinGen Allele Registry
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Canonical Allele Identifier:
CA308888765
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.44912383G>C
GRCh37
chr19:g.45415640G>C
Linked Data - NCBI & NCI
dbSNP:
445925
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.44912383G>C , CM000681.2:g.44912383G>C
GRCh38
NC_000019.9:g.45415640G>C , CM000681.1:g.45415640G>C
GRCh37
NC_000019.8:g.50107480G>C
NCBI36
NG_012859.1:g.2720G>C
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