Canonical Allele Identifier: CA353362088

Gene: PDHB

Linked Data

• MyVariant Identifiers: chr3:g.58416566C>G (hg19) ; chr3:g.58430839C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.58430839C>G , CM000665.2:g.58430839C>G	GRCh38
NC_000003.11:g.58416566C>G , CM000665.1:g.58416566C>G	GRCh37
NC_000003.10:g.58391606C>G	NCBI36
NG_016860.1:g.8014G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302746.11:c.407G>C MANE Select	ENSP00000307241.6:p.Gly136Ala
ENST00000302746.10:c.407G>C	ENSP00000307241.6:p.Gly136Ala
ENST00000383714.8:c.353G>C	ENSP00000373220.4:p.Gly118Ala
ENST00000461692.5:n.520G>C
ENST00000469364.5:c.407G>C	ENSP00000419580.1:p.Gly136Ala
ENST00000474765.1:c.353G>C	ENSP00000418448.1:p.Gly118Ala
ENST00000479945.1:n.2812G>C
ENST00000480626.5:n.499G>C
ENST00000485460.5:c.403+4G>C	ENSP00000417267.1:n.403+4G>C
NM_000925.3:c.407G>C	NP_000916.2:p.Gly136Ala
NM_001173468.1:c.403+4G>C	NP_001166939.1:n.403+4G>C
NM_001315536.1:c.353G>C	NP_001302465.1:p.Gly118Ala
NR_033384.1:n.520G>C
NM_000925.4:c.407G>C MANE Select	NP_000916.2:p.Gly136Ala
NM_001173468.2:c.403+4G>C	NP_001166939.1:n.403+4G>C
NM_001315536.2:c.353G>C	NP_001302465.1:p.Gly118Ala
NR_033384.2:n.513G>C