Canonical Allele Identifier: CA434867111
Gene: DCBLD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.98600409T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.98881565T>C , CM000665.2:g.98881565T>C GRCh38
NC_000003.11:g.98600409T>C , CM000665.1:g.98600409T>C GRCh37
NC_000003.10:g.100083099T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000326840.11:c.408A>G MANE Select ENSP00000321573.6:p.Gly136=
ENST00000326840.10:c.408A>G ENSP00000321573.6:p.Gly136=
ENST00000326857.9:c.408A>G ENSP00000321646.9:p.Gly136=
ENST00000449482.1:c.90A>G ENSP00000396803.1:p.Gly30=
ENST00000469648.5:n.268+19157A>G
ENST00000486004.1:n.386A>G
NM_080927.3:c.408A>G NP_563615.3:p.Gly136=
XM_011512419.1:c.205+19557A>G XP_011510721.1:n.205+19557A>G
XM_011512419.2:c.205+19557A>G XP_011510721.1:n.205+19557A>G
XM_024453347.1:c.90A>G XP_024309115.1:p.Gly30=
XM_024453348.1:c.90A>G XP_024309116.1:p.Gly30=
NM_080927.4:c.408A>G MANE Select NP_563615.3:p.Gly136=