Canonical Allele Identifier: CA805554654

Gene: PPARGC1B

Linked Data

• dbSNP Id: rs1361012488
• MyVariant Identifiers: chr5:g.149202654G>C (hg19) ; chr5:g.149823091G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149823091G>C , CM000667.2:g.149823091G>C	GRCh38
NC_000005.9:g.149202654G>C , CM000667.1:g.149202654G>C	GRCh37
NC_000005.8:g.149182847G>C	NCBI36
NG_016747.1:g.97840G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309241.10:c.252+2485G>C MANE Select	ENSP00000312649.5:n.252+2485G>C
ENST00000309241.9:c.252+2485G>C	ENSP00000312649.5:n.252+2485G>C
ENST00000360453.8:c.252+2485G>C	ENSP00000353638.4:n.252+2485G>C
ENST00000394320.7:c.252+2485G>C	ENSP00000377855.3:n.252+2485G>C
ENST00000403750.5:c.177+2485G>C	ENSP00000384403.1:n.177+2485G>C
NM_001172698.1:c.252+2485G>C	NP_001166169.1:n.252+2485G>C
NM_001172699.1:c.177+2485G>C	NP_001166170.1:n.177+2485G>C
NM_133263.3:c.252+2485G>C	NP_573570.3:n.252+2485G>C
XM_005268372.3:c.189+2485G>C	XP_005268429.1:n.189+2485G>C
XM_011537553.1:c.252+2485G>C	XP_011535855.1:n.252+2485G>C
XM_011537554.1:c.189+2485G>C	XP_011535856.1:n.189+2485G>C
XM_011537555.1:c.252+2485G>C	XP_011535857.1:n.252+2485G>C
XM_011537556.1:c.-244+2485G>C	XP_011535858.1:n.-244+2485G>C
XM_011537557.1:c.252+2485G>C	XP_011535859.1:n.252+2485G>C
XM_005268372.4:c.189+2485G>C	XP_005268429.1:n.189+2485G>C
XM_011537553.2:c.252+2485G>C	XP_011535855.1:n.252+2485G>C
XM_011537554.2:c.189+2485G>C	XP_011535856.1:n.189+2485G>C
XM_011537555.2:c.252+2485G>C	XP_011535857.1:n.252+2485G>C
XM_011537556.2:c.-244+2485G>C	XP_011535858.1:n.-244+2485G>C
NM_133263.4:c.252+2485G>C MANE Select	NP_573570.3:n.252+2485G>C
NM_001172698.2:c.252+2485G>C	NP_001166169.1:n.252+2485G>C
NM_001172699.2:c.177+2485G>C	NP_001166170.1:n.177+2485G>C