Canonical Allele Identifier: CA1088249397
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1772001793
gnomAD v3: 6-41751251-G-A
gnomAD v4: 6-41751251-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751251G>A , CM000668.2:g.41751251G>A GRCh38
NC_000006.11:g.41718989G>A , CM000668.1:g.41718989G>A GRCh37
NC_000006.10:g.41826967G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2647C>T ENSP00000399429.1:n.71+2647C>T
Search 100 bp 5'
Search 100 bp 3'