Canonical Allele Identifier: CA743845705
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs819169
MyVariant Identifiers: chr20:g.32868037G>T (hg19) chr20:g.34280231G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34280231G>T , CM000682.2:g.34280231G>T GRCh38
NC_000020.10:g.32868037G>T , CM000682.1:g.32868037G>T GRCh37
NC_000020.9:g.32331698G>T NCBI36
NG_012630.1:g.36572C>A
NG_012630.2:g.36572C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+796C>A XP_011526959.1:n.*7+796C>A
XM_011528658.1:c.*7+796C>A XP_011526960.1:n.*7+796C>A
XM_011528657.2:c.*7+796C>A XP_011526959.2:n.*7+796C>A
XM_011528658.3:c.*7+796C>A XP_011526960.2:n.*7+796C>A
XM_017027709.2:c.*7+796C>A XP_016883198.1:n.*7+796C>A
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