ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA525390624
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.113761105C>T
GRCh37
chr1:g.114303727C>T
Linked Data - Sequence & Population
gnomAD v2:
1:114303727 C / T
gnomAD v3:
1:113761105 C / T
gnomAD v4:
chr1-113761105-C-T
Linked Data - NCBI & NCI
dbSNP:
1355826412
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.113761105C>T , CM000663.2:g.113761105C>T
GRCh38
NC_000001.10:g.114303727C>T , CM000663.1:g.114303727C>T
GRCh37
NC_000001.9:g.114105250C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'