Canonical Allele Identifier: CA340528064

Gene: TACSTD2

Linked Data

• MyVariant Identifiers: chr1:g.59042567T>C (hg19) ; chr1:g.58576895T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58576895T>C , CM000663.2:g.58576895T>C	GRCh38
NC_000001.10:g.59042567T>C , CM000663.1:g.59042567T>C	GRCh37
NC_000001.9:g.58815155T>C	NCBI36
NG_016237.1:g.5600A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.262A>G MANE Select	ENSP00000360269.2:p.Thr88Ala
ENST00000371225.3:c.262A>G	ENSP00000360269.2:p.Thr88Ala
NM_002353.2:c.262A>G	NP_002344.2:p.Thr88Ala
NM_002353.3:c.262A>G MANE Select	NP_002344.2:p.Thr88Ala