Canonical Allele Identifier: CA2646760106

Gene: DBT

Linked Data

• gnomAD v4: 1-100206120-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100206120G>T , CM000663.2:g.100206120G>T	GRCh38
NC_000001.10:g.100671676G>T , CM000663.1:g.100671676G>T	GRCh37
NC_000001.9:g.100444264G>T	NCBI36
NG_011852.2:g.48734C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681617.1:c.1407+110C>A	ENSP00000505544.1:n.1407+110C>A
ENST00000681780.1:c.738+110C>A	ENSP00000505780.1:n.738+110C>A
ENST00000370132.8:c.1281+110C>A MANE Select	ENSP00000359151.3:n.1281+110C>A
NM_001918.3:c.1281+110C>A	NP_001909.3:n.1281+110C>A
XM_005270545.2:c.738+110C>A	XP_005270602.1:n.738+110C>A
XM_005270546.2:c.738+110C>A	XP_005270603.1:n.738+110C>A
XM_005270545.4:c.738+110C>A	XP_005270602.1:n.738+110C>A
XM_017000468.2:c.738+110C>A	XP_016855957.1:n.738+110C>A
XM_017000469.2:c.738+110C>A	XP_016855958.1:n.738+110C>A
NM_001918.4:c.1281+110C>A	NP_001909.3:n.1281+110C>A
NM_001918.5:c.1281+110C>A MANE Select	NP_001909.4:n.1281+110C>A
NM_001399969.1:c.738+110C>A	NP_001386898.1:n.738+110C>A
NM_001399972.1:c.738+110C>A	NP_001386901.1:n.738+110C>A
NR_174363.1:n.1113+110C>A
NR_174364.1:n.1295+110C>A
NR_174365.1:n.1078+110C>A
NR_174366.1:n.1380+110C>A