Canonical Allele Identifier: CA2361127888
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs142598970
gnomAD v4: 20-34269365-T-C
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Genomic Alleles

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

Transcript Alleles

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