ClinGen Allele Registry
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Canonical Allele Identifier:
CA261560051
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.57549696C>A
GRCh37
chr14:g.58016414C>A
Linked Data - Sequence & Population
gnomAD v3:
14:57549696 C / A
gnomAD v4:
chr14-57549696-C-A
Linked Data - NCBI & NCI
dbSNP:
1495465
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.57549696C>A , CM000676.2:g.57549696C>A
GRCh38
NC_000014.8:g.58016414C>A , CM000676.1:g.58016414C>A
GRCh37
NC_000014.7:g.57086167C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'