Canonical Allele Identifier: CA1017103726
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs1601623930
gnomAD v3: 20-34269361-T-A
gnomAD v4: 20-34269361-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34269361T>A , CM000682.2:g.34269361T>A GRCh38
NC_000020.10:g.32857167T>A , CM000682.1:g.32857167T>A GRCh37
NC_000020.9:g.32320828T>A NCBI36
NG_011439.1:g.13997T>A

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+11666A>T XP_011526959.1:n.*7+11666A>T
XM_011528657.2:c.*7+11666A>T XP_011526959.2:n.*7+11666A>T
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