Canonical Allele Identifier: CA103492204
Gene: DKK2 HGNC NCBI

Linked Data

dbSNP Id: rs447372
gnomAD v2: 4-107853996-G-A
gnomAD v3: 4-106932839-G-A
gnomAD v4: 4-106932839-G-A
MyVariant Identifiers: chr4:g.107853996G>A (hg19) chr4:g.106932839G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.106932839G>A , CM000666.2:g.106932839G>A GRCh38
NC_000004.11:g.107853996G>A , CM000666.1:g.107853996G>A GRCh37
NC_000004.10:g.108073445G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000285311.8:c.223-6890C>T MANE Select ENSP00000285311.3:n.223-6890C>T
ENST00000285311.7:c.223-6890C>T ENSP00000285311.3:n.223-6890C>T
ENST00000510463.1:c.85-6890C>T ENSP00000423797.1:n.85-6890C>T
ENST00000510534.1:n.444-6890C>T
ENST00000513208.5:c.-78-6890C>T ENSP00000421255.1:n.-78-6890C>T
NM_014421.2:c.223-6890C>T NP_055236.1:n.223-6890C>T
NM_014421.3:c.223-6890C>T MANE Select NP_055236.1:n.223-6890C>T
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