Canonical Allele Identifier: CA824781348
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs1401137980
gnomAD v3: 6-41751235-C-T
gnomAD v4: 6-41751235-C-T
MyVariant Identifiers: chr6:g.41718973C>T (hg19) chr6:g.41751235C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751235C>T , CM000668.2:g.41751235C>T GRCh38
NC_000006.11:g.41718973C>T , CM000668.1:g.41718973C>T GRCh37
NC_000006.10:g.41826951C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2663G>A ENSP00000399429.1:n.71+2663G>A
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