Canonical Allele Identifier: CA340526780
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs80358223
MyVariant Identifiers: chr1:g.59042477G>C (hg19) chr1:g.58576805G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576805G>C , CM000663.2:g.58576805G>C GRCh38
NC_000001.10:g.59042477G>C , CM000663.1:g.59042477G>C GRCh37
NC_000001.9:g.58815065G>C NCBI36
NG_016237.1:g.5690C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371225.4:c.352C>G MANE Select ENSP00000360269.2:p.Gln118Glu
ENST00000371225.3:c.352C>G ENSP00000360269.2:p.Gln118Glu
NM_002353.2:c.352C>G NP_002344.2:p.Gln118Glu
NM_002353.3:c.352C>G MANE Select NP_002344.2:p.Gln118Glu
Search 100 bp 5'
Search 100 bp 3'