ClinGen Allele Registry
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Canonical Allele Identifier:
CA794886201
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr4:g.41282694T>A
GRCh37
chr4:g.41284711T>A
Linked Data - Sequence & Population
gnomAD v3:
4:41282694 T / A
gnomAD v4:
chr4-41282694-T-A
Linked Data - NCBI & NCI
dbSNP:
4861096
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.41282694T>A , CM000666.2:g.41282694T>A
GRCh38
NC_000004.11:g.41284711T>A , CM000666.1:g.41284711T>A
GRCh37
NC_000004.10:g.40979468T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'