Canonical Allele Identifier: CA418182960
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs1646886559
MyVariant Identifiers: chr1:g.59042481C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576809C>T , CM000663.2:g.58576809C>T GRCh38
NC_000001.10:g.59042481C>T , CM000663.1:g.59042481C>T GRCh37
NC_000001.9:g.58815069C>T NCBI36
NG_016237.1:g.5686G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.348G>A MANE Select ENSP00000360269.2:p.Ala116=
ENST00000371225.3:c.348G>A ENSP00000360269.2:p.Ala116=
NM_002353.2:c.348G>A NP_002344.2:p.Ala116=
NM_002353.3:c.348G>A MANE Select NP_002344.2:p.Ala116=
Search 100 bp 5'
Search 100 bp 3'