Canonical Allele Identifier: CA784231626

Gene: DCBLD2

Linked Data

• dbSNP Id: rs1304282300
• gnomAD v3: 3-98881356-G-A
• gnomAD v4: 3-98881356-G-A
• MyVariant Identifiers: chr3:g.98600200G>A (hg19) ; chr3:g.98881356G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.98881356G>A , CM000665.2:g.98881356G>A	GRCh38
NC_000003.11:g.98600200G>A , CM000665.1:g.98600200G>A	GRCh37
NC_000003.10:g.100082890G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326840.11:c.433+184C>T MANE Select	ENSP00000321573.6:n.433+184C>T
ENST00000326840.10:c.433+184C>T	ENSP00000321573.6:n.433+184C>T
ENST00000326857.9:c.433+184C>T	ENSP00000321646.9:n.433+184C>T
ENST00000449482.1:c.115+184C>T	ENSP00000396803.1:n.115+184C>T
ENST00000469648.5:n.268+19366C>T
ENST00000486004.1:n.411+184C>T
NM_080927.3:c.433+184C>T	NP_563615.3:n.433+184C>T
XM_011512419.1:c.205+19766C>T	XP_011510721.1:n.205+19766C>T
XM_011512419.2:c.205+19766C>T	XP_011510721.1:n.205+19766C>T
XM_024453347.1:c.115+184C>T	XP_024309115.1:n.115+184C>T
XM_024453348.1:c.115+184C>T	XP_024309116.1:n.115+184C>T
NM_080927.4:c.433+184C>T MANE Select	NP_563615.3:n.433+184C>T