Canonical Allele Identifier: CA1623760100
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1772000529
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751119T>A , CM000668.2:g.41751119T>A GRCh38
NC_000006.11:g.41718857T>A , CM000668.1:g.41718857T>A GRCh37
NC_000006.10:g.41826835T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2779A>T ENSP00000399429.1:n.71+2779A>T
Search 100 bp 5'
Search 100 bp 3'