Canonical Allele Identifier: CA1623760219
Gene: PGC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751217T= , CM000668.2:g.41751217T= GRCh38
NC_000006.11:g.41718955T= , CM000668.1:g.41718955T= GRCh37
NC_000006.10:g.41826933T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2681A= ENSP00000399429.1:n.71+2681A=