Canonical Allele Identifier: CA635305365
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs1285357504
gnomAD v2: 20-32857153-A-C
gnomAD v3: 20-34269347-A-C
gnomAD v4: 20-34269347-A-C
MyVariant Identifiers: chr20:g.32857153A>C (hg19) chr20:g.34269347A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34269347A>C , CM000682.2:g.34269347A>C GRCh38
NC_000020.10:g.32857153A>C , CM000682.1:g.32857153A>C GRCh37
NC_000020.9:g.32320814A>C NCBI36
NG_011439.1:g.13983A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+11680T>G XP_011526959.1:n.*7+11680T>G
XM_011528657.2:c.*7+11680T>G XP_011526959.2:n.*7+11680T>G
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