Canonical Allele Identifier: CA138085867

Gene: PGC

Linked Data

• dbSNP Id: rs1033964907
• gnomAD v3: 6-41751186-C-T
• gnomAD v4: 6-41751186-C-T
• MyVariant Identifiers: chr6:g.41718924C>T (hg19) ; chr6:g.41751186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41751186C>T , CM000668.2:g.41751186C>T	GRCh38
NC_000006.11:g.41718924C>T , CM000668.1:g.41718924C>T	GRCh37
NC_000006.10:g.41826902C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415707.1:c.71+2712G>A	ENSP00000399429.1:n.71+2712G>A