ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA577544620
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.119966578C>A
GRCh37
chr7:g.119606632C>A
Linked Data - Sequence & Population
gnomAD v2:
7:119606632 C / A
gnomAD v3:
7:119966578 C / A
gnomAD v4:
chr7-119966578-C-A
Linked Data - NCBI & NCI
dbSNP:
17142462
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.119966578C>A , CM000669.2:g.119966578C>A
GRCh38
NC_000007.13:g.119606632C>A , CM000669.1:g.119606632C>A
GRCh37
NC_000007.12:g.119393868C>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'