Canonical Allele Identifier: CA313334837
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs142598970
gnomAD v3: 20-34269365-T-G
gnomAD v4: 20-34269365-T-G
MyVariant Identifiers: chr20:g.32857171T>G (hg19) chr20:g.34269365T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34269365T>G , CM000682.2:g.34269365T>G GRCh38
NC_000020.10:g.32857171T>G , CM000682.1:g.32857171T>G GRCh37
NC_000020.9:g.32320832T>G NCBI36
NG_011439.1:g.14001T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+11662A>C XP_011526959.1:n.*7+11662A>C
XM_011528657.2:c.*7+11662A>C XP_011526959.2:n.*7+11662A>C
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