ClinGen Allele Registry
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Canonical Allele Identifier:
CA14073385
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.25649511C>T
GRCh37
chr15:g.25894658C>T
Linked Data - Sequence & Population
gnomAD v2:
15:25894658 C / T
gnomAD v3:
15:25649511 C / T
gnomAD v4:
chr15-25649511-C-T
Joint Max Group AF
0.6082413 (AFR)
Genomes Max Group AF
0.6082413 (AFR)
Linked Data - NCBI & NCI
dbSNP:
6576443
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.25649511C>T , CM000677.2:g.25649511C>T
GRCh38
NC_000015.9:g.25894658C>T , CM000677.1:g.25894658C>T
GRCh37
NC_000015.8:g.23445751C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'