ClinGen Allele Registry
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Canonical Allele Identifier:
CA158385494
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.46713893C>T
Linked Data - Sequence & Population
gnomAD v3:
7:46713893 C / T
gnomAD v4:
chr7-46713893-C-T
Linked Data - NCBI & NCI
dbSNP:
700750
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.46713893C>T , CM000669.2:g.46713893C>T
GRCh38
NC_000007.13:g.46753491C>T , CM000669.1:g.46753491C>T
GRCh37
NC_000007.12:g.46720016C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'