Canonical Allele Identifier: CA743840951
Gene: AHCY HGNC NCBI

Linked Data

dbSNP Id: rs1449139221
MyVariant Identifiers: chr20:g.32857152_32857154del (hg19) chr20:g.34269346_34269348del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.34269347_34269349del , CM000682.2:g.34269347_34269349del GRCh38
NC_000020.10:g.32857153_32857155del , CM000682.1:g.32857153_32857155del GRCh37
NC_000020.9:g.32320814_32320816del NCBI36
NG_011439.1:g.13983_13985del

Transcript Alleles

HGVS Amino-acid Change
XM_011528657.1:c.*7+11679_*7+11681del XP_011526959.1:n.*7+11679_*7+11681del
XM_011528657.2:c.*7+11679_*7+11681del XP_011526959.2:n.*7+11679_*7+11681del
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