Canonical Allele Identifier: CA626456449
Gene: ZNF652-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1381185095
gnomAD v2: 17-47440451-AAG-A
gnomAD v3: 17-49363089-AAG-A
gnomAD v4: 17-49363089-AAG-A
MyVariant Identifiers: chr17:g.47440452_47440453del (hg19) chr17:g.49363090_49363091del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49363094_49363095del , CM000679.2:g.49363094_49363095del GRCh38
NC_000017.10:g.47440456_47440457del , CM000679.1:g.47440456_47440457del GRCh37
NC_000017.9:g.44795455_44795456del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110882.1:n.136+577_136+578del
NR_110883.1:n.31-1185_31-1184del
NR_110884.1:n.58-1185_58-1184del
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