Canonical Allele Identifier: CA103521902
Gene: DKK2 HGNC NCBI

Linked Data

dbSNP Id: rs770563947
gnomAD v2: 4-108115075-A-G
gnomAD v3: 4-107193918-A-G
gnomAD v4: 4-107193918-A-G
MyVariant Identifiers: chr4:g.108115075A>G (hg19) chr4:g.107193918A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.107193918A>G , CM000666.2:g.107193918A>G GRCh38
NC_000004.11:g.108115075A>G , CM000666.1:g.108115075A>G GRCh37
NC_000004.10:g.108334524A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000510463.1:c.-83-5393T>C ENSP00000423797.1:n.-83-5393T>C
ENST00000513208.5:c.-177-5393T>C ENSP00000421255.1:n.-177-5393T>C
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