Canonical Allele Identifier: CA340525922
Gene: TACSTD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59042395C>A (hg19) chr1:g.58576723C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576723C>A , CM000663.2:g.58576723C>A GRCh38
NC_000001.10:g.59042395C>A , CM000663.1:g.59042395C>A GRCh37
NC_000001.9:g.58814983C>A NCBI36
NG_016237.1:g.5772G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.434G>T MANE Select ENSP00000360269.2:p.Cys145Phe
ENST00000371225.3:c.434G>T ENSP00000360269.2:p.Cys145Phe
NM_002353.2:c.434G>T NP_002344.2:p.Cys145Phe
NM_002353.3:c.434G>T MANE Select NP_002344.2:p.Cys145Phe
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