ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA783226134
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1107050G>A
GRCh37
chr19:g.1107049G>A
Linked Data - Sequence & Population
gnomAD v3:
19:1107050 G / A
gnomAD v4:
chr19-1107050-G-A
Linked Data - NCBI & NCI
dbSNP:
1282874105
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1107050G>A , CM000681.2:g.1107050G>A
GRCh38
NC_000019.9:g.1107049G>A , CM000681.1:g.1107049G>A
GRCh37
NC_000019.8:g.1058049G>A
NCBI36
NG_050621.1:g.8125G>A
Search 100 bp 5'
Search 100 bp 3'