ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA14661463
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.40990556T>C
GRCh37
chr19:g.41496461T>C
Linked Data - Sequence & Population
gnomAD v2:
19:41496461 T / C
gnomAD v3:
19:40990556 T / C
gnomAD v4:
chr19-40990556-T-C
Joint Max Group AF
0.89295795 (AFR)
Genomes Max Group AF
0.89295795 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4802101
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.40990556T>C , CM000681.2:g.40990556T>C
GRCh38
NC_000019.9:g.41496461T>C , CM000681.1:g.41496461T>C
GRCh37
NC_000019.8:g.46188301T>C
NCBI36
NG_007929.1:g.4258T>C
Search 100 bp 5'
Search 100 bp 3'