Canonical Allele Identifier: CA877452
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs775384382
ExAC: 1:59042536 A / T
gnomAD v2: 1-59042536-A-T
gnomAD v4: 1-58576864-A-T
MyVariant Identifiers: chr1:g.59042536A>T (hg19) chr1:g.58576864A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576864A>T , CM000663.2:g.58576864A>T GRCh38
NC_000001.10:g.59042536A>T , CM000663.1:g.59042536A>T GRCh37
NC_000001.9:g.58815124A>T NCBI36
NG_016237.1:g.5631T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.293T>A MANE Select ENSP00000360269.2:p.Val98Glu
ENST00000371225.3:c.293T>A ENSP00000360269.2:p.Val98Glu
NM_002353.2:c.293T>A NP_002344.2:p.Val98Glu
NM_002353.3:c.293T>A MANE Select NP_002344.2:p.Val98Glu
Search 100 bp 5'
Search 100 bp 3'