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Canonical Allele Identifier:
CA13909998
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.42382485C>T
GRCh37
chr13:g.42956621C>T
Linked Data - Sequence & Population
gnomAD v2:
13:42956621 C / T
gnomAD v3:
13:42382485 C / T
gnomAD v4:
chr13-42382485-C-T
Joint Max Group AF
0.12447858 (SAS)
Genomes Max Group AF
0.12447858 (SAS)
Linked Data - NCBI & NCI
dbSNP:
17638544
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.42382485C>T , CM000675.2:g.42382485C>T
GRCh38
NC_000013.10:g.42956621C>T , CM000675.1:g.42956621C>T
GRCh37
NC_000013.9:g.41854621C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'