Canonical Allele Identifier: CA340525905

Gene: TACSTD2

Linked Data

• dbSNP Id: rs1646885565
• MyVariant Identifiers: chr1:g.59042393C>G (hg19) ; chr1:g.58576721C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58576721C>G , CM000663.2:g.58576721C>G	GRCh38
NC_000001.10:g.59042393C>G , CM000663.1:g.59042393C>G	GRCh37
NC_000001.9:g.58814981C>G	NCBI36
NG_016237.1:g.5774G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.436G>C MANE Select	ENSP00000360269.2:p.Asp146His
ENST00000371225.3:c.436G>C	ENSP00000360269.2:p.Asp146His
NM_002353.2:c.436G>C	NP_002344.2:p.Asp146His
NM_002353.3:c.436G>C MANE Select	NP_002344.2:p.Asp146His