Canonical Allele Identifier: CA340526063
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs1646885811
gnomAD v4: 1-58576741-C-T
MyVariant Identifiers: chr1:g.59042413C>T (hg19) chr1:g.58576741C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576741C>T , CM000663.2:g.58576741C>T GRCh38
NC_000001.10:g.59042413C>T , CM000663.1:g.59042413C>T GRCh37
NC_000001.9:g.58815001C>T NCBI36
NG_016237.1:g.5754G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.416G>A MANE Select ENSP00000360269.2:p.Gly139Asp
ENST00000371225.3:c.416G>A ENSP00000360269.2:p.Gly139Asp
NM_002353.2:c.416G>A NP_002344.2:p.Gly139Asp
NM_002353.3:c.416G>A MANE Select NP_002344.2:p.Gly139Asp
Search 100 bp 5'
Search 100 bp 3'