Canonical Allele Identifier: CA307288385
Gene: TSHZ3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs779462471
gnomAD v2: 19-31911147-C-T
gnomAD v3: 19-31420241-C-T
gnomAD v4: 19-31420241-C-T
MyVariant Identifiers: chr19:g.31911147C>T (hg19) chr19:g.31420241C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.31420241C>T , CM000681.2:g.31420241C>T GRCh38
NC_000019.9:g.31911147C>T , CM000681.1:g.31911147C>T GRCh37
NC_000019.8:g.36602987C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001753896.1:n.2902C>T
XR_001753897.1:n.2898C>T
XR_001753898.1:n.2898C>T
XR_001753899.1:n.2622C>T
XR_001753900.1:n.2394C>T
XR_002958388.1:n.3024C>T
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