Canonical Allele Identifier: CA2739275142

Gene: DBT

Linked Data

• ClinVar Variation Id: 2820071
• ClinVar RCV Id: RCV003637199

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206313A>C , CM000663.2:g.100206313A>C	GRCh38
NC_000001.10:g.100671869A>C , CM000663.1:g.100671869A>C	GRCh37
NC_000001.9:g.100444457A>C	NCBI36
NG_011852.2:g.48541T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.1336-12T>G	ENSP00000505544.1:n.1336-12T>G
ENST00000681780.1:c.667-12T>G	ENSP00000505780.1:n.667-12T>G
ENST00000370132.8:c.1210-12T>G MANE Select	ENSP00000359151.3:n.1210-12T>G
NM_001918.3:c.1210-12T>G	NP_001909.3:n.1210-12T>G
XM_005270545.2:c.667-12T>G	XP_005270602.1:n.667-12T>G
XM_005270546.2:c.667-12T>G	XP_005270603.1:n.667-12T>G
XM_005270545.4:c.667-12T>G	XP_005270602.1:n.667-12T>G
XM_017000468.2:c.667-12T>G	XP_016855957.1:n.667-12T>G
XM_017000469.2:c.667-12T>G	XP_016855958.1:n.667-12T>G
NM_001918.4:c.1210-12T>G	NP_001909.3:n.1210-12T>G
NM_001918.5:c.1210-12T>G MANE Select	NP_001909.4:n.1210-12T>G
NM_001399969.1:c.667-12T>G	NP_001386898.1:n.667-12T>G
NM_001399972.1:c.667-12T>G	NP_001386901.1:n.667-12T>G
NR_174363.1:n.1042-12T>G
NR_174364.1:n.1224-12T>G
NR_174365.1:n.1007-12T>G
NR_174366.1:n.1309-12T>G