ClinGen Allele Registry
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Canonical Allele Identifier:
CA695273165
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.113105720T>G
GRCh37
chr13:g.113760034T>G
Linked Data - Sequence & Population
gnomAD v4:
chr13-113105720-T-G
Linked Data - NCBI & NCI
dbSNP:
561241
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.113105720T>G , CM000675.2:g.113105720T>G
GRCh38
NC_000013.10:g.113760034T>G , CM000675.1:g.113760034T>G
GRCh37
NC_000013.9:g.112808035T>G
NCBI36
NG_009262.1:g.4930T>G , LRG_554:g.4930T>G
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