Canonical Allele Identifier: CA2361127875
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs2035847622
gnomAD v4: 20-34269345-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34269345C>A , CM000682.2:g.34269345C>A GRCh38
NC_000020.10:g.32857151C>A , CM000682.1:g.32857151C>A GRCh37
NC_000020.9:g.32320812C>A NCBI36
NG_011439.1:g.13981C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+11682G>T XP_011526959.1:n.*7+11682G>T
XM_011528657.2:c.*7+11682G>T XP_011526959.2:n.*7+11682G>T
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