Canonical Allele Identifier: CA877323

Gene: TACSTD2

Linked Data

• ClinVar Variation Id: 297766
• ClinVar RCV Id: RCV000386862 ; RCV003546502 ; RCV004021444
• dbSNP Id: rs769179472
• ExAC: 1:59042002 C / T
• gnomAD v2: 1-59042002-C-T
• gnomAD v3: 1-58576330-C-T
• gnomAD v4: 1-58576330-C-T
• MyVariant Identifiers: chr1:g.59042002C>T (hg19) ; chr1:g.58576330C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58576330C>T , CM000663.2:g.58576330C>T	GRCh38
NC_000001.10:g.59042002C>T , CM000663.1:g.59042002C>T	GRCh37
NC_000001.9:g.58814590C>T	NCBI36
NG_016237.1:g.6165G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.827G>A MANE Select	ENSP00000360269.2:p.Gly276Asp
ENST00000371225.3:c.827G>A	ENSP00000360269.2:p.Gly276Asp
NM_002353.2:c.827G>A	NP_002344.2:p.Gly276Asp
NM_002353.3:c.827G>A MANE Select	NP_002344.2:p.Gly276Asp