Canonical Allele Identifier: CA13366721
Gene: WBP1L HGNC NCBI

Linked Data

dbSNP Id: rs10883782
gnomAD v2: 10-104583932-A-G
gnomAD v3: 10-102824175-A-G
gnomAD v4: 10-102824175-A-G
MyVariant Identifiers: chr10:g.104583932A>G (hg19) chr10:g.102824175A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102824175A>G , CM000672.2:g.102824175A>G GRCh38
NC_000010.10:g.104583932A>G , CM000672.1:g.104583932A>G GRCh37
NC_000010.9:g.104573922A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000647664.1:c.*300+1843A>G ENSP00000498131.1:n.*300+1843A>G
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