ClinGen Allele Registry
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Canonical Allele Identifier:
CA690835390
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr12:g.6342424A>G
GRCh37
chr12:g.6451590A>G
Linked Data - NCBI & NCI
dbSNP:
4149570
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.6342424A>G , CM000674.2:g.6342424A>G
GRCh38
NC_000012.11:g.6451590A>G , CM000674.1:g.6451590A>G
GRCh37
NC_000012.10:g.6321851A>G
NCBI36
NG_007506.1:g.4672T>C , LRG_193:g.4672T>C
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