Canonical Allele Identifier: CA418182976
Gene: TACSTD2 HGNC NCBI

Linked Data

gnomAD v4: 1-58576818-G-T
MyVariant Identifiers: chr1:g.59042490G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576818G>T , CM000663.2:g.58576818G>T GRCh38
NC_000001.10:g.59042490G>T , CM000663.1:g.59042490G>T GRCh37
NC_000001.9:g.58815078G>T NCBI36
NG_016237.1:g.5677C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.339C>A MANE Select ENSP00000360269.2:p.Arg113=
ENST00000371225.3:c.339C>A ENSP00000360269.2:p.Arg113=
NM_002353.2:c.339C>A NP_002344.2:p.Arg113=
NM_002353.3:c.339C>A MANE Select NP_002344.2:p.Arg113=
Search 100 bp 5'
Search 100 bp 3'