ClinGen Allele Registry
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Canonical Allele Identifier:
CA10849035
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.159387894T>C
GRCh37
chr1:g.159357684T>C
Linked Data - Sequence & Population
gnomAD v2:
1:159357684 T / C
gnomAD v3:
1:159387894 T / C
gnomAD v4:
chr1-159387894-T-C
Joint Max Group AF
0.81323433 (AFR)
Genomes Max Group AF
0.81323433 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4446959
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.159387894T>C , CM000663.2:g.159387894T>C
GRCh38
NC_000001.10:g.159357684T>C , CM000663.1:g.159357684T>C
GRCh37
NC_000001.9:g.157624308T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'