Canonical Allele Identifier: CA1387545225
Gene: DCBLD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98881541T= , CM000665.2:g.98881541T= GRCh38
NC_000003.11:g.98600385T= , CM000665.1:g.98600385T= GRCh37
NC_000003.10:g.100083075T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326840.11:c.432A= MANE Select ENSP00000321573.6:p.Ile144=
ENST00000326840.10:c.432A= ENSP00000321573.6:p.Ile144=
ENST00000326857.9:c.432A= ENSP00000321646.9:p.Ile144=
ENST00000449482.1:c.114A= ENSP00000396803.1:p.Ile38=
ENST00000469648.5:n.268+19181A=
ENST00000486004.1:n.410A=
NM_080927.3:c.432A= NP_563615.3:p.Ile144=
XM_011512419.1:c.205+19581A= XP_011510721.1:n.205+19581A=
XM_011512419.2:c.205+19581A= XP_011510721.1:n.205+19581A=
XM_024453347.1:c.114A= XP_024309115.1:p.Ile38=
XM_024453348.1:c.114A= XP_024309116.1:p.Ile38=
NM_080927.4:c.432A= MANE Select NP_563615.3:p.Ile144=