Canonical Allele Identifier: CA1623760132
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1470329080
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751144G>A , CM000668.2:g.41751144G>A GRCh38
NC_000006.11:g.41718882G>A , CM000668.1:g.41718882G>A GRCh37
NC_000006.10:g.41826860G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2754C>T ENSP00000399429.1:n.71+2754C>T
Search 100 bp 5'
Search 100 bp 3'