ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15352850
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.154613256T>C
GRCh37
chr4:g.155534408T>C
Linked Data - Sequence & Population
gnomAD v2:
4:155534408 T / C
gnomAD v3:
4:154613256 T / C
gnomAD v4:
chr4-154613256-T-C
Joint Max Group AF
0.44566001 (NFE)
Genomes Max Group AF
0.44566001 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1800792
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.154613256T>C , CM000666.2:g.154613256T>C
GRCh38
NC_000004.11:g.155534408T>C , CM000666.1:g.155534408T>C
GRCh37
NC_000004.10:g.155753858T>C
NCBI36
NG_008834.1:g.4495A>G
Search 100 bp 5'
Search 100 bp 3'