ClinGen Allele Registry
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Canonical Allele Identifier:
CA15379874
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.159337169T>C
GRCh37
chr5:g.158764177T>C
Linked Data - Sequence & Population
gnomAD v2:
5:158764177 T / C
gnomAD v3:
5:159337169 T / C
gnomAD v4:
chr5-159337169-T-C
Joint Max Group AF
0.46378792 (EAS)
Genomes Max Group AF
0.46378792 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7709212
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.159337169T>C , CM000667.2:g.159337169T>C
GRCh38
NC_000005.9:g.158764177T>C , CM000667.1:g.158764177T>C
GRCh37
NC_000005.8:g.158696755T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_037889.1:n.745+4166T>C
Search 100 bp 5'
Search 100 bp 3'