ClinGen Allele Registry
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Canonical Allele Identifier:
CA691234066
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.68160508G>A
GRCh37
chr12:g.68554288G>A
Linked Data - NCBI & NCI
dbSNP:
2069707
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.68160508G>A , CM000674.2:g.68160508G>A
GRCh38
NC_000012.11:g.68554288G>A , CM000674.1:g.68554288G>A
GRCh37
NC_000012.10:g.66840555G>A
NCBI36
NG_015840.1:g.4234C>T
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