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Canonical Allele Identifier:
CA585077701
Gene: CASC11
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr8:g.127705823G>A
GRCh37
chr8:g.128718068G>A
Linked Data - Sequence & Population
gnomAD v2:
8:128718068 G / A
gnomAD v3:
8:127705823 G / A
gnomAD v4:
chr8-127705823-G-A
Joint Max Group AF
0.00007905 (AFR)
Genomes Max Group AF
0.00007905 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9642880
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.127705823G>A , CM000670.2:g.127705823G>A
GRCh38
NC_000008.10:g.128718068G>A , CM000670.1:g.128718068G>A
GRCh37
NC_000008.9:g.128787250G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_117102.1:n.366-2580C>T
Search 100 bp 5'
Search 100 bp 3'