ClinGen Allele Registry
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Canonical Allele Identifier:
CA12219184
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.166993145G>C
GRCh37
chr6:g.167406633G>C
Linked Data - Sequence & Population
gnomAD v2:
6:167406633 G / C
gnomAD v3:
6:166993145 G / C
gnomAD v4:
chr6-166993145-G-C
Joint Max Group AF
0.52783707 (NFE)
Genomes Max Group AF
0.52783707 (NFE)
Linked Data - NCBI & NCI
dbSNP:
415890
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.166993145G>C , CM000668.2:g.166993145G>C
GRCh38
NC_000006.11:g.167406633G>C , CM000668.1:g.167406633G>C
GRCh37
NC_000006.10:g.167326623G>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'