Canonical Allele Identifier: CA1623760157
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1772000927

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751169T>C , CM000668.2:g.41751169T>C GRCh38
NC_000006.11:g.41718907T>C , CM000668.1:g.41718907T>C GRCh37
NC_000006.10:g.41826885T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2729A>G ENSP00000399429.1:n.71+2729A>G