Canonical Allele Identifier: CA1590644786

Gene: PPARGC1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149771108G= , CM000667.2:g.149771108G=	GRCh38
NC_000005.9:g.149150671G= , CM000667.1:g.149150671G=	GRCh37
NC_000005.8:g.149130864G=	NCBI36
NG_016747.1:g.45857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309241.10:c.78+40688G= MANE Select	ENSP00000312649.5:n.78+40688G=
ENST00000309241.9:c.78+40688G=	ENSP00000312649.5:n.78+40688G=
ENST00000360453.8:c.78+40688G=	ENSP00000353638.4:n.78+40688G=
ENST00000394320.7:c.78+40688G=	ENSP00000377855.3:n.78+40688G=
ENST00000461780.1:n.432+9496G=
NM_001172698.1:c.78+40688G=	NP_001166169.1:n.78+40688G=
NM_133263.3:c.78+40688G=	NP_573570.3:n.78+40688G=
XM_011537553.1:c.78+40688G=	XP_011535855.1:n.78+40688G=
XM_011537555.1:c.78+40688G=	XP_011535857.1:n.78+40688G=
XM_011537557.1:c.78+40688G=	XP_011535859.1:n.78+40688G=
XM_011537553.2:c.78+40688G=	XP_011535855.1:n.78+40688G=
XM_011537555.2:c.78+40688G=	XP_011535857.1:n.78+40688G=
NM_133263.4:c.78+40688G= MANE Select	NP_573570.3:n.78+40688G=
NM_001172698.2:c.78+40688G=	NP_001166169.1:n.78+40688G=