ClinGen Allele Registry
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Canonical Allele Identifier:
CA344464
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.169765160G>C
GRCh37
chr3:g.169482948G>C
Linked Data - NCBI & NCI
ClinVar Allele:
49824
ClinVar RCV:
RCV000034302
ClinVar Variation:
41400
dbSNP:
199422256
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.169765160G>C , CM000665.2:g.169765160G>C
GRCh38
NC_000003.11:g.169482948G>C , CM000665.1:g.169482948G>C
GRCh37
NC_000003.10:g.170965642G>C
NCBI36
NG_016363.1:g.4901C>G , LRG_347:g.4901C>G
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