Canonical Allele Identifier: CA566748549
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1333662262
gnomAD v2: 6-41718852-C-A
gnomAD v3: 6-41751114-C-A
gnomAD v4: 6-41751114-C-A
MyVariant Identifiers: chr6:g.41718852C>A (hg19) chr6:g.41751114C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751114C>A , CM000668.2:g.41751114C>A GRCh38
NC_000006.11:g.41718852C>A , CM000668.1:g.41718852C>A GRCh37
NC_000006.10:g.41826830C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2784G>T ENSP00000399429.1:n.71+2784G>T
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