ClinGen Allele Registry
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Canonical Allele Identifier:
CA14657145
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.18021731T>C
GRCh37
chr19:g.18132540T>C
Linked Data - Sequence & Population
gnomAD v2:
19:18132540 T / C
gnomAD v3:
19:18021731 T / C
gnomAD v4:
chr19-18021731-T-C
Joint Max Group AF
0.11930083 (NFE)
Genomes Max Group AF
0.11930083 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12984174
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.18021731T>C , CM000681.2:g.18021731T>C
GRCh38
NC_000019.9:g.18132540T>C , CM000681.1:g.18132540T>C
GRCh37
NC_000019.8:g.17993540T>C
NCBI36
Search 100 bp 5'
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