Canonical Allele Identifier: CA340527366
Gene: TACSTD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59042524C>A (hg19) chr1:g.58576852C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576852C>A , CM000663.2:g.58576852C>A GRCh38
NC_000001.10:g.59042524C>A , CM000663.1:g.59042524C>A GRCh37
NC_000001.9:g.58815112C>A NCBI36
NG_016237.1:g.5643G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.305G>T MANE Select ENSP00000360269.2:p.Gly102Val
ENST00000371225.3:c.305G>T ENSP00000360269.2:p.Gly102Val
NM_002353.2:c.305G>T NP_002344.2:p.Gly102Val
NM_002353.3:c.305G>T MANE Select NP_002344.2:p.Gly102Val
Search 100 bp 5'
Search 100 bp 3'