Canonical Allele Identifier: CA312100282
Gene: ISM1 HGNC NCBI
TASP1 HGNC NCBI

Linked Data

dbSNP Id: rs542668297
MyVariant Identifiers: chr20:g.13296896A>C (hg19) chr20:g.13316249A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316249A>C , CM000682.2:g.13316249A>C GRCh38
NC_000020.10:g.13296896A>C , CM000682.1:g.13296896A>C GRCh37
NC_000020.9:g.13244896A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-194T>G
XM_017027680.1:c.878-8817A>C (ISM1) XP_016883169.1:n.878-8817A>C
XR_001754319.2:n.1282-194T>G (TASP1)
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