Canonical Allele Identifier: CA1623760121
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1772000627

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751136C>G , CM000668.2:g.41751136C>G GRCh38
NC_000006.11:g.41718874C>G , CM000668.1:g.41718874C>G GRCh37
NC_000006.10:g.41826852C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2762G>C ENSP00000399429.1:n.71+2762G>C