ClinGen Allele Registry
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Canonical Allele Identifier:
CA15517698
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr7:g.97388483G>A
GRCh37
chr7:g.97017795G>A
Linked Data - Sequence & Population
gnomAD v2:
7:97017795 G / A
gnomAD v3:
7:97388483 G / A
gnomAD v4:
chr7-97388483-G-A
Joint Max Group AF
0.29241697 (AFR)
Genomes Max Group AF
0.29241697 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10255878
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.97388483G>A , CM000669.2:g.97388483G>A
GRCh38
NC_000007.13:g.97017795G>A , CM000669.1:g.97017795G>A
GRCh37
NC_000007.12:g.96855731G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001745293.1:n.127-59836C>T
Search 100 bp 5'
Search 100 bp 3'