Canonical Allele Identifier: CA2595897902

Gene: PGC

Linked Data

• dbSNP Id: rs2127294337
• gnomAD v3: 6-41751211-T-C
• gnomAD v4: 6-41751211-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41751211T>C , CM000668.2:g.41751211T>C	GRCh38
NC_000006.11:g.41718949T>C , CM000668.1:g.41718949T>C	GRCh37
NC_000006.10:g.41826927T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415707.1:c.71+2687A>G	ENSP00000399429.1:n.71+2687A>G