Canonical Allele Identifier: CA312100300
Gene: ISM1 HGNC NCBI
TASP1 HGNC NCBI

Linked Data

dbSNP Id: rs987531623
MyVariant Identifiers: chr20:g.13296969C>A (hg19) chr20:g.13316322C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316322C>A , CM000682.2:g.13316322C>A GRCh38
NC_000020.10:g.13296969C>A , CM000682.1:g.13296969C>A GRCh37
NC_000020.9:g.13244969C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937280.1:n.601-267G>T
XM_017027680.1:c.878-8744C>A (ISM1) XP_016883169.1:n.878-8744C>A
XR_001754319.2:n.1282-267G>T (TASP1)
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