Canonical Allele Identifier: CA824781307
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1385749651
gnomAD v3: 6-41751139-A-C
gnomAD v4: 6-41751139-A-C
MyVariant Identifiers: chr6:g.41718877A>C (hg19) chr6:g.41751139A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751139A>C , CM000668.2:g.41751139A>C GRCh38
NC_000006.11:g.41718877A>C , CM000668.1:g.41718877A>C GRCh37
NC_000006.10:g.41826855A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2759T>G ENSP00000399429.1:n.71+2759T>G
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