Canonical Allele Identifier: CA340523871
Gene: TACSTD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59042122A>T (hg19) chr1:g.58576450A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576450A>T , CM000663.2:g.58576450A>T GRCh38
NC_000001.10:g.59042122A>T , CM000663.1:g.59042122A>T GRCh37
NC_000001.9:g.58814710A>T NCBI36
NG_016237.1:g.6045T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371225.4:c.707T>A MANE Select ENSP00000360269.2:p.Phe236Tyr
ENST00000371225.3:c.707T>A ENSP00000360269.2:p.Phe236Tyr
NM_002353.2:c.707T>A NP_002344.2:p.Phe236Tyr
NM_002353.3:c.707T>A MANE Select NP_002344.2:p.Phe236Tyr
Search 100 bp 5'
Search 100 bp 3'