Canonical Allele Identifier: CA340527980

Gene: TACSTD2

Linked Data

• gnomAD v4: 1-58576888-A-C
• MyVariant Identifiers: chr1:g.59042560A>C (hg19) ; chr1:g.58576888A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58576888A>C , CM000663.2:g.58576888A>C	GRCh38
NC_000001.10:g.59042560A>C , CM000663.1:g.59042560A>C	GRCh37
NC_000001.9:g.58815148A>C	NCBI36
NG_016237.1:g.5607T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.269T>G MANE Select	ENSP00000360269.2:p.Val90Gly
ENST00000371225.3:c.269T>G	ENSP00000360269.2:p.Val90Gly
NM_002353.2:c.269T>G	NP_002344.2:p.Val90Gly
NM_002353.3:c.269T>G MANE Select	NP_002344.2:p.Val90Gly