Canonical Allele Identifier: CA1387545123
Gene: DCBLD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98881449A= , CM000665.2:g.98881449A= GRCh38
NC_000003.11:g.98600293A= , CM000665.1:g.98600293A= GRCh37
NC_000003.10:g.100082983A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326840.11:c.433+91T= MANE Select ENSP00000321573.6:n.433+91T=
ENST00000326840.10:c.433+91T= ENSP00000321573.6:n.433+91T=
ENST00000326857.9:c.433+91T= ENSP00000321646.9:n.433+91T=
ENST00000449482.1:c.115+91T= ENSP00000396803.1:n.115+91T=
ENST00000469648.5:n.268+19273T=
ENST00000486004.1:n.411+91T=
NM_080927.3:c.433+91T= NP_563615.3:n.433+91T=
XM_011512419.1:c.205+19673T= XP_011510721.1:n.205+19673T=
XM_011512419.2:c.205+19673T= XP_011510721.1:n.205+19673T=
XM_024453347.1:c.115+91T= XP_024309115.1:n.115+91T=
XM_024453348.1:c.115+91T= XP_024309116.1:n.115+91T=
NM_080927.4:c.433+91T= MANE Select NP_563615.3:n.433+91T=