Canonical Allele Identifier: CA1590672465

Gene: PPARGC1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149832680G= , CM000667.2:g.149832680G=	GRCh38
NC_000005.9:g.149212243G= , CM000667.1:g.149212243G=	GRCh37
NC_000005.8:g.149192436G=	NCBI36
NG_016747.1:g.107429G=

Transcript Alleles

HGVS	Amino-acid Change
NM_133263.4:c.607G= MANE Select	NP_573570.3:p.Ala203=
ENST00000309241.10:c.607G= MANE Select	ENSP00000312649.5:p.Ala203=
NM_001172698.1:c.490G=	NP_001166169.1:p.Ala164=
NM_001172698.2:c.490G=	NP_001166169.1:p.Ala164=
NM_001172699.1:c.415G=	NP_001166170.1:p.Ala139=
NM_001172699.2:c.415G=	NP_001166170.1:p.Ala139=
NM_133263.3:c.607G=	NP_573570.3:p.Ala203=
ENST00000309241.9:c.607G=	ENSP00000312649.5:p.Ala203=
ENST00000360453.8:c.490G=	ENSP00000353638.4:p.Ala164=
ENST00000394320.7:c.607G=	ENSP00000377855.3:p.Ala203=
ENST00000403750.5:c.415G=	ENSP00000384403.1:p.Ala139=
XM_005268372.3:c.544G=	XP_005268429.1:p.Ala182=
XM_005268372.4:c.544G=	XP_005268429.1:p.Ala182=
XM_011537553.1:c.607G=	XP_011535855.1:p.Ala203=
XM_011537553.2:c.607G=	XP_011535855.1:p.Ala203=
XM_011537554.1:c.544G=	XP_011535856.1:p.Ala182=
XM_011537554.2:c.544G=	XP_011535856.1:p.Ala182=
XM_011537555.1:c.490G=	XP_011535857.1:p.Ala164=
XM_011537555.2:c.490G=	XP_011535857.1:p.Ala164=
XM_011537556.1:c.-6G=	XP_011535858.1:n.-6G=
XM_011537556.2:c.-6G=	XP_011535858.1:n.-6G=
XM_011537557.1:c.607G=	XP_011535859.1:p.Ala203=