Canonical Allele Identifier: CA1387545119
Gene: DCBLD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98881445C= , CM000665.2:g.98881445C= GRCh38
NC_000003.11:g.98600289C= , CM000665.1:g.98600289C= GRCh37
NC_000003.10:g.100082979C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326840.11:c.433+95G= MANE Select ENSP00000321573.6:n.433+95G=
ENST00000326840.10:c.433+95G= ENSP00000321573.6:n.433+95G=
ENST00000326857.9:c.433+95G= ENSP00000321646.9:n.433+95G=
ENST00000449482.1:c.115+95G= ENSP00000396803.1:n.115+95G=
ENST00000469648.5:n.268+19277G=
ENST00000486004.1:n.411+95G=
NM_080927.3:c.433+95G= NP_563615.3:n.433+95G=
XM_011512419.1:c.205+19677G= XP_011510721.1:n.205+19677G=
XM_011512419.2:c.205+19677G= XP_011510721.1:n.205+19677G=
XM_024453347.1:c.115+95G= XP_024309115.1:n.115+95G=
XM_024453348.1:c.115+95G= XP_024309116.1:n.115+95G=
NM_080927.4:c.433+95G= MANE Select NP_563615.3:n.433+95G=