Allele Registry

Canonical Allele Identifier: CA95792999

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr4:g.41282694T>C

GRCh37 chr4:g.41284711T>C

Linked Data - Sequence & Population

gnomAD v2:

4:41284711 T / C

gnomAD v3:

4:41282694 T / C

gnomAD v4:

chr4-41282694-T-C

Joint Max Group AF 0.519021 (EAS)

Genomes Max Group AF 0.519021 (EAS)

Linked Data - NCBI & NCI

dbSNP:

4861096

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.41282694T>C , CM000666.2:g.41282694T>C	GRCh38
NC_000004.11:g.41284711T>C , CM000666.1:g.41284711T>C	GRCh37
NC_000004.10:g.40979468T>C	NCBI36

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