Canonical Allele Identifier: CA313334828
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs545199987
gnomAD v3: 20-34269349-G-A
gnomAD v4: 20-34269349-G-A
MyVariant Identifiers: chr20:g.32857155G>A (hg19) chr20:g.34269349G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34269349G>A , CM000682.2:g.34269349G>A GRCh38
NC_000020.10:g.32857155G>A , CM000682.1:g.32857155G>A GRCh37
NC_000020.9:g.32320816G>A NCBI36
NG_011439.1:g.13985G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+11678C>T XP_011526959.1:n.*7+11678C>T
XM_011528657.2:c.*7+11678C>T XP_011526959.2:n.*7+11678C>T
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