ClinGen Allele Registry
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Canonical Allele Identifier:
CA199140204
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.117525430G>A
GRCh37
chr9:g.120287708G>A
Linked Data - Sequence & Population
gnomAD v3:
9:117525430 G / A
gnomAD v4:
chr9-117525430-G-A
Linked Data - NCBI & NCI
dbSNP:
2771051
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.117525430G>A , CM000671.2:g.117525430G>A
GRCh38
NC_000009.11:g.120287708G>A , CM000671.1:g.120287708G>A
GRCh37
NC_000009.10:g.119327529G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'