ClinGen Allele Registry
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Canonical Allele Identifier:
CA476374737
Gene: DISC1FP1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr11:g.90853732C>A
GRCh37
chr11:g.90586900C>A
Linked Data - NCBI & NCI
dbSNP:
12274302
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.90853732C>A , CM000673.2:g.90853732C>A
GRCh38
NC_000011.9:g.90586900C>A , CM000673.1:g.90586900C>A
GRCh37
NC_000011.8:g.90226548C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_104190.1:n.591+1025C>A
Search 100 bp 5'
Search 100 bp 3'