Canonical Allele Identifier: CA340526381
Gene: TACSTD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59042444T>G (hg19) chr1:g.58576772T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576772T>G , CM000663.2:g.58576772T>G GRCh38
NC_000001.10:g.59042444T>G , CM000663.1:g.59042444T>G GRCh37
NC_000001.9:g.58815032T>G NCBI36
NG_016237.1:g.5723A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.385A>C MANE Select ENSP00000360269.2:p.Asn129His
ENST00000371225.3:c.385A>C ENSP00000360269.2:p.Asn129His
NM_002353.2:c.385A>C NP_002344.2:p.Asn129His
NM_002353.3:c.385A>C MANE Select NP_002344.2:p.Asn129His
Search 100 bp 5'
Search 100 bp 3'