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Canonical Allele Identifier:
CA476374738
Gene: DISC1FP1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.90853732C>G
GRCh37
chr11:g.90586900C>G
Linked Data - Sequence & Population
gnomAD v2:
11:90586900 C / G
gnomAD v3:
11:90853732 C / G
gnomAD v4:
chr11-90853732-C-G
Joint Max Group AF
0.00004813 (AFR)
Genomes Max Group AF
0.00004813 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12274302
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.90853732C>G , CM000673.2:g.90853732C>G
GRCh38
NC_000011.9:g.90586900C>G , CM000673.1:g.90586900C>G
GRCh37
NC_000011.8:g.90226548C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104190.1:n.591+1025C>G
Search 100 bp 5'
Search 100 bp 3'