Canonical Allele Identifier: CA307288368
Gene: TSHZ3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1020457019
gnomAD v2: 19-31911053-G-A
gnomAD v3: 19-31420147-G-A
gnomAD v4: 19-31420147-G-A
MyVariant Identifiers: chr19:g.31911053G>A (hg19) chr19:g.31420147G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.31420147G>A , CM000681.2:g.31420147G>A GRCh38
NC_000019.9:g.31911053G>A , CM000681.1:g.31911053G>A GRCh37
NC_000019.8:g.36602893G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753896.1:n.2808G>A
XR_001753897.1:n.2804G>A
XR_001753898.1:n.2804G>A
XR_001753899.1:n.2528G>A
XR_001753900.1:n.2300G>A
XR_002958388.1:n.2930G>A
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