Allele Registry

Canonical Allele Identifier: CA11843164

Gene: F11-AS1 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr4:g.186336422A>G

GRCh37 chr4:g.187257576A>G

Linked Data - Sequence & Population

gnomAD v2:

4:187257576 A / G

gnomAD v3:

4:186336422 A / G

gnomAD v4:

chr4-186336422-A-G

Joint Max Group AF 0.25036208 (NFE)

Genomes Max Group AF 0.25036208 (NFE)

Linked Data - NCBI & NCI

dbSNP:

13148903

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186336422A>G , CM000666.2:g.186336422A>G	GRCh38
NC_000004.11:g.187257576A>G , CM000666.1:g.187257576A>G	GRCh37
NC_000004.10:g.187494570A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033900.1:n.215-45390T>C

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