Canonical Allele Identifier: CA784993888
Gene: DKK2 HGNC NCBI

Linked Data

dbSNP Id: rs1325763274
MyVariant Identifiers: chr4:g.107853958T>G (hg19) chr4:g.106932801T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.106932801T>G , CM000666.2:g.106932801T>G GRCh38
NC_000004.11:g.107853958T>G , CM000666.1:g.107853958T>G GRCh37
NC_000004.10:g.108073407T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000285311.8:c.223-6852A>C MANE Select ENSP00000285311.3:n.223-6852A>C
ENST00000285311.7:c.223-6852A>C ENSP00000285311.3:n.223-6852A>C
ENST00000510463.1:c.85-6852A>C ENSP00000423797.1:n.85-6852A>C
ENST00000510534.1:n.444-6852A>C
ENST00000513208.5:c.-78-6852A>C ENSP00000421255.1:n.-78-6852A>C
NM_014421.2:c.223-6852A>C NP_055236.1:n.223-6852A>C
NM_014421.3:c.223-6852A>C MANE Select NP_055236.1:n.223-6852A>C
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