Canonical Allele Identifier: CA340525905
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs1646885565
MyVariant Identifiers: chr1:g.59042393C>G (hg19) chr1:g.58576721C>G (hg38)
JSON-LD

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
Search 100 bp 5'
Search 100 bp 3'