ClinGen Allele Registry
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Canonical Allele Identifier:
CA772051964
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.41741012A>G
GRCh37
chr17:g.39897264A>G
Linked Data - NCBI & NCI
dbSNP:
6503659
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.41741012A>G , CM000679.2:g.41741012A>G
GRCh38
NC_000017.10:g.39897264A>G , CM000679.1:g.39897264A>G
GRCh37
NC_000017.9:g.37150790A>G
NCBI36
NG_009090.2:g.50701T>C , LRG_401:g.50701T>C
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