Canonical Allele Identifier: CA632965700
Gene: TSHZ3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1161378999
gnomAD v2: 19-31911109-T-A
gnomAD v3: 19-31420203-T-A
gnomAD v4: 19-31420203-T-A
MyVariant Identifiers: chr19:g.31911109T>A (hg19) chr19:g.31420203T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.31420203T>A , CM000681.2:g.31420203T>A GRCh38
NC_000019.9:g.31911109T>A , CM000681.1:g.31911109T>A GRCh37
NC_000019.8:g.36602949T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001753896.1:n.2864T>A
XR_001753897.1:n.2860T>A
XR_001753898.1:n.2860T>A
XR_001753899.1:n.2584T>A
XR_001753900.1:n.2356T>A
XR_002958388.1:n.2986T>A
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