Allele Registry

Canonical Allele Identifier: CA15651841

Gene: WBP1L HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr10:g.102821531A>C

GRCh37 chr10:g.104581288A>C

Linked Data - Sequence & Population

gnomAD v2:

10:104581288 A / C

gnomAD v3:

10:102821531 A / C

gnomAD v4:

chr10-102821531-A-C

Joint Max Group AF 0.55513685 (NFE)

Genomes Max Group AF 0.55513685 (NFE)

Linked Data - NCBI & NCI

dbSNP:

619824

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102821531A>C , CM000672.2:g.102821531A>C	GRCh38
NC_000010.10:g.104581288A>C , CM000672.1:g.104581288A>C	GRCh37
NC_000010.9:g.104571278A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647664.1:c.442+228A>C	ENSP00000498131.1:n.442+228A>C

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