Canonical Allele Identifier: CA553882051
Gene: DKK2 HGNC NCBI

Linked Data

dbSNP Id: rs1432322814
gnomAD v2: 4-107853932-G-A
gnomAD v3: 4-106932775-G-A
gnomAD v4: 4-106932775-G-A
MyVariant Identifiers: chr4:g.107853932G>A (hg19) chr4:g.106932775G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.106932775G>A , CM000666.2:g.106932775G>A GRCh38
NC_000004.11:g.107853932G>A , CM000666.1:g.107853932G>A GRCh37
NC_000004.10:g.108073381G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000285311.8:c.223-6826C>T MANE Select ENSP00000285311.3:n.223-6826C>T
ENST00000285311.7:c.223-6826C>T ENSP00000285311.3:n.223-6826C>T
ENST00000510463.1:c.85-6826C>T ENSP00000423797.1:n.85-6826C>T
ENST00000510534.1:n.444-6826C>T
ENST00000513208.5:c.-78-6826C>T ENSP00000421255.1:n.-78-6826C>T
NM_014421.2:c.223-6826C>T NP_055236.1:n.223-6826C>T
NM_014421.3:c.223-6826C>T MANE Select NP_055236.1:n.223-6826C>T
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