Allele Registry

Canonical Allele Identifier: CA30877353

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr1:g.155162859T>C

GRCh37 chr1:g.155135335T>C

Linked Data - Sequence & Population

gnomAD v2:

1:155135335 T / C

gnomAD v3:

1:155162859 T / C

gnomAD v4:

chr1-155162859-T-C

Joint Max Group AF 0.78296132 (EAS)

Genomes Max Group AF 0.78296132 (EAS)

Linked Data - NCBI & NCI

dbSNP:

4460629

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155162859T>C , CM000663.2:g.155162859T>C	GRCh38
NC_000001.10:g.155135335T>C , CM000663.1:g.155135335T>C	GRCh37
NC_000001.9:g.153401959T>C	NCBI36

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