Canonical Allele Identifier: CA418182872
Gene: TACSTD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59042418G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576746G>A , CM000663.2:g.58576746G>A GRCh38
NC_000001.10:g.59042418G>A , CM000663.1:g.59042418G>A GRCh37
NC_000001.9:g.58815006G>A NCBI36
NG_016237.1:g.5749C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.411C>T MANE Select ENSP00000360269.2:p.Asp137=
ENST00000371225.3:c.411C>T ENSP00000360269.2:p.Asp137=
NM_002353.2:c.411C>T NP_002344.2:p.Asp137=
NM_002353.3:c.411C>T MANE Select NP_002344.2:p.Asp137=
Search 100 bp 5'
Search 100 bp 3'