Canonical Allele Identifier: CA1169462498
Gene: TACSTD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576799T= , CM000663.2:g.58576799T= GRCh38
NC_000001.10:g.59042471T= , CM000663.1:g.59042471T= GRCh37
NC_000001.9:g.58815059T= NCBI36
NG_016237.1:g.5696A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.358A= MANE Select ENSP00000360269.2:p.Asn120=
ENST00000371225.3:c.358A= ENSP00000360269.2:p.Asn120=
NM_002353.2:c.358A= NP_002344.2:p.Asn120=
NM_002353.3:c.358A= MANE Select NP_002344.2:p.Asn120=
Search 100 bp 5'
Search 100 bp 3'