Canonical Allele Identifier: CA1623760104
Gene: PGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751120A= , CM000668.2:g.41751120A= GRCh38
NC_000006.11:g.41718858A= , CM000668.1:g.41718858A= GRCh37
NC_000006.10:g.41826836A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2778T= ENSP00000399429.1:n.71+2778T=