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Canonical Allele Identifier:
CA143522266
Gene: CASC6
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.91664050C>T
GRCh37
chr6:g.92373768C>T
Linked Data - Sequence & Population
gnomAD v2:
6:92373768 C / T
gnomAD v3:
6:91664050 C / T
gnomAD v4:
chr6-91664050-C-T
Joint Max Group AF
0.00018202 (NFE)
Genomes Max Group AF
0.00018202 (NFE)
Linked Data - NCBI & NCI
dbSNP:
28416183
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.91664050C>T , CM000668.2:g.91664050C>T
GRCh38
NC_000006.11:g.92373768C>T , CM000668.1:g.92373768C>T
GRCh37
NC_000006.10:g.92430489C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104154.1:n.263+20998G>A
Search 100 bp 5'
Search 100 bp 3'