ClinGen Allele Registry
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Canonical Allele Identifier:
CA158322468
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.46202985T>A
GRCh37
chr7:g.46242583T>A
Linked Data - Sequence & Population
gnomAD v3:
7:46202985 T / A
gnomAD v4:
chr7-46202985-T-A
Linked Data - NCBI & NCI
dbSNP:
6964415
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.46202985T>A , CM000669.2:g.46202985T>A
GRCh38
NC_000007.13:g.46242583T>A , CM000669.1:g.46242583T>A
GRCh37
NC_000007.12:g.46209108T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'