Canonical Allele Identifier: CA12039213
Gene: PPARGC1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149731403A>C , CM000667.2:g.149731403A>C GRCh38
NC_000005.9:g.149110966A>C , CM000667.1:g.149110966A>C GRCh37
NC_000005.8:g.149091159A>C NCBI36
NG_016747.1:g.6152A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309241.10:c.78+983A>C MANE Select ENSP00000312649.5:n.78+983A>C
ENST00000309241.9:c.78+983A>C ENSP00000312649.5:n.78+983A>C
ENST00000360453.8:c.78+983A>C ENSP00000353638.4:n.78+983A>C
ENST00000394320.7:c.78+983A>C ENSP00000377855.3:n.78+983A>C
ENST00000461780.1:n.118+983A>C
NM_001172698.1:c.78+983A>C NP_001166169.1:n.78+983A>C
NM_133263.3:c.78+983A>C NP_573570.3:n.78+983A>C
XM_011537553.1:c.78+983A>C XP_011535855.1:n.78+983A>C
XM_011537555.1:c.78+983A>C XP_011535857.1:n.78+983A>C
XM_011537557.1:c.78+983A>C XP_011535859.1:n.78+983A>C
XM_011537553.2:c.78+983A>C XP_011535855.1:n.78+983A>C
XM_011537555.2:c.78+983A>C XP_011535857.1:n.78+983A>C
NM_133263.4:c.78+983A>C MANE Select NP_573570.3:n.78+983A>C
NM_001172698.2:c.78+983A>C NP_001166169.1:n.78+983A>C
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