Canonical Allele Identifier: CA312100276
Gene: ISM1 HGNC NCBI
TASP1 HGNC NCBI

Linked Data

dbSNP Id: rs937302898
MyVariant Identifiers: chr20:g.13296810T>A (hg19) chr20:g.13316163T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316163T>A , CM000682.2:g.13316163T>A GRCh38
NC_000020.10:g.13296810T>A , CM000682.1:g.13296810T>A GRCh37
NC_000020.9:g.13244810T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-108A>T
XM_017027680.1:c.878-8903T>A (ISM1) XP_016883169.1:n.878-8903T>A
XR_001754319.2:n.1282-108A>T (TASP1)
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