Canonical Allele Identifier: CA138085836
Gene: PGC HGNC NCBI

Linked Data

dbSNP Id: rs114680079
gnomAD v2: 6-41718900-A-T
gnomAD v3: 6-41751162-A-T
gnomAD v4: 6-41751162-A-T
MyVariant Identifiers: chr6:g.41718900A>T (hg19) chr6:g.41751162A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41751162A>T , CM000668.2:g.41751162A>T GRCh38
NC_000006.11:g.41718900A>T , CM000668.1:g.41718900A>T GRCh37
NC_000006.10:g.41826878A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000415707.1:c.71+2736T>A ENSP00000399429.1:n.71+2736T>A
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