ClinGen Allele Registry
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Canonical Allele Identifier:
CA863142974
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.3128341C>T
GRCh37
chr9:g.3128341C>T
Linked Data - Sequence & Population
gnomAD v3:
9:3128341 C / T
gnomAD v4:
chr9-3128341-C-T
Linked Data - NCBI & NCI
dbSNP:
1478788509
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.3128341C>T , CM000671.2:g.3128341C>T
GRCh38
NC_000009.11:g.3128341C>T , CM000671.1:g.3128341C>T
GRCh37
NC_000009.10:g.3118341C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'