ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA535763659
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.120365807T>A
GRCh37
chr2:g.121123383T>A
Linked Data - Sequence & Population
gnomAD v2:
2:121123383 T / A
gnomAD v3:
2:120365807 T / A
gnomAD v4:
chr2-120365807-T-A
Linked Data - NCBI & NCI
dbSNP:
12711941
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.120365807T>A , CM000664.2:g.120365807T>A
GRCh38
NC_000002.11:g.121123383T>A , CM000664.1:g.121123383T>A
GRCh37
NC_000002.10:g.120839853T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'