Canonical Allele Identifier: CA634719557
Gene: ISM1 HGNC NCBI
TASP1 HGNC NCBI

Linked Data

dbSNP Id: rs1205667502
gnomAD v2: 20-13296757-A-G
gnomAD v3: 20-13316110-A-G
gnomAD v4: 20-13316110-A-G
MyVariant Identifiers: chr20:g.13296757A>G (hg19) chr20:g.13316110A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.13316110A>G , CM000682.2:g.13316110A>G GRCh38
NC_000020.10:g.13296757A>G , CM000682.1:g.13296757A>G GRCh37
NC_000020.9:g.13244757A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937280.1:n.601-55T>C
XM_017027680.1:c.878-8956A>G (ISM1) XP_016883169.1:n.878-8956A>G
XR_001754319.2:n.1282-55T>C (TASP1)
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