Canonical Allele Identifier: CA1623760200
Gene: PGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751200C= , CM000668.2:g.41751200C= GRCh38
NC_000006.11:g.41718938C= , CM000668.1:g.41718938C= GRCh37
NC_000006.10:g.41826916C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2698G= ENSP00000399429.1:n.71+2698G=