Canonical Allele Identifier: CA313334832
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs754982015
gnomAD v2: 20-32857162-G-A
gnomAD v3: 20-34269356-G-A
gnomAD v4: 20-34269356-G-A
MyVariant Identifiers: chr20:g.32857162G>A (hg19) chr20:g.34269356G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34269356G>A , CM000682.2:g.34269356G>A GRCh38
NC_000020.10:g.32857162G>A , CM000682.1:g.32857162G>A GRCh37
NC_000020.9:g.32320823G>A NCBI36
NG_011439.1:g.13992G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+11671C>T XP_011526959.1:n.*7+11671C>T
XM_011528657.2:c.*7+11671C>T XP_011526959.2:n.*7+11671C>T
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