Canonical Allele Identifier: CA434040233

Gene: PDHB

Linked Data

• ClinVar Variation Id: 2854564
• ClinVar RCV Id: RCV003628593
• MyVariant Identifiers: chr3:g.58416493C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58430766C>T , CM000665.2:g.58430766C>T	GRCh38
NC_000003.11:g.58416493C>T , CM000665.1:g.58416493C>T	GRCh37
NC_000003.10:g.58391533C>T	NCBI36
NG_016860.1:g.8087G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.480G>A MANE Select	ENSP00000307241.6:p.Gln160=
ENST00000302746.10:c.480G>A	ENSP00000307241.6:p.Gln160=
ENST00000383714.8:c.426G>A	ENSP00000373220.4:p.Gln142=
ENST00000461692.5:n.593G>A
ENST00000469364.5:c.480G>A	ENSP00000419580.1:p.Gln160=
ENST00000474765.1:c.426G>A	ENSP00000418448.1:p.Gln142=
ENST00000479945.1:n.2885G>A
ENST00000480626.5:n.572G>A
ENST00000485460.5:c.426G>A	ENSP00000417267.1:p.Gln142=
NM_000925.3:c.480G>A	NP_000916.2:p.Gln160=
NM_001173468.1:c.426G>A	NP_001166939.1:p.Gln142=
NM_001315536.1:c.426G>A	NP_001302465.1:p.Gln142=
NR_033384.1:n.593G>A
NM_000925.4:c.480G>A MANE Select	NP_000916.2:p.Gln160=
NM_001173468.2:c.426G>A	NP_001166939.1:p.Gln142=
NM_001315536.2:c.426G>A	NP_001302465.1:p.Gln142=
NR_033384.2:n.586G>A