Canonical Allele Identifier: CA636039238
Gene: SLC12A5-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs11476145
gnomAD v2: 20-44645266-C-CAA
gnomAD v3: 20-46016627-C-CAA
gnomAD v4: 20-46016627-C-CAA
MyVariant Identifiers: chr20:g.44645270_44645271insAA (hg19) chr20:g.44645266_44645267insAA (hg19) chr20:g.46016631_46016632insAA (hg38) chr20:g.46016627_46016628insAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46016643_46016644dup , CM000682.2:g.46016643_46016644dup GRCh38
NC_000020.10:g.44645282_44645283dup , CM000682.1:g.44645282_44645283dup GRCh37
NC_000020.9:g.44078689_44078690dup NCBI36
NG_011468.1:g.12736_12737dup

Transcript Alleles

HGVS Amino-acid Change
NR_147699.1:n.669-1841_669-1840dup
Search 100 bp 5'
Search 100 bp 3'