Canonical Allele Identifier: CA12294940
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs9471643
gnomAD v2: 6-41718915-G-C
gnomAD v3: 6-41751177-G-C
gnomAD v4: 6-41751177-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751177G>C , CM000668.2:g.41751177G>C GRCh38
NC_000006.11:g.41718915G>C , CM000668.1:g.41718915G>C GRCh37
NC_000006.10:g.41826893G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000415707.1:c.71+2721C>G ENSP00000399429.1:n.71+2721C>G