Canonical Allele Identifier: CA340526061

Gene: TACSTD2

Linked Data

• MyVariant Identifiers: chr1:g.59042413C>G (hg19) ; chr1:g.58576741C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.416G>C MANE Select	ENSP00000360269.2:p.Gly139Ala
ENST00000371225.3:c.416G>C	ENSP00000360269.2:p.Gly139Ala
NM_002353.2:c.416G>C	NP_002344.2:p.Gly139Ala
NM_002353.3:c.416G>C MANE Select	NP_002344.2:p.Gly139Ala