Canonical Allele Identifier: CA636039250
Gene: SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1190244701
gnomAD v2: 20-44645291-CAAAT-C
gnomAD v3: 20-46016652-CAAAT-C
gnomAD v4: 20-46016652-CAAAT-C
MyVariant Identifiers: chr20:g.44645292_44645295del (hg19) chr20:g.46016653_46016656del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016655_46016658del , CM000682.2:g.46016655_46016658del GRCh38
NC_000020.10:g.44645294_44645297del , CM000682.1:g.44645294_44645297del GRCh37
NC_000020.9:g.44078701_44078704del NCBI36
NG_011468.1:g.12748_12751del

Transcript Alleles

HGVS Amino-acid Change
NR_147699.1:n.669-1868_669-1865del
Search 100 bp 5'
Search 100 bp 3'