ClinGen Allele Registry
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Canonical Allele Identifier:
CA13976996
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.48556315C>T
GRCh37
chr14:g.49025518C>T
Linked Data - Sequence & Population
gnomAD v2:
14:49025518 C / T
gnomAD v3:
14:48556315 C / T
gnomAD v4:
chr14-48556315-C-T
Joint Max Group AF
0.18461067 (NFE)
Genomes Max Group AF
0.18461067 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4522336
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.48556315C>T , CM000676.2:g.48556315C>T
GRCh38
NC_000014.8:g.49025518C>T , CM000676.1:g.49025518C>T
GRCh37
NC_000014.7:g.48095268C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001750756.1:n.585-127072G>A
Search 100 bp 5'
Search 100 bp 3'