Canonical Allele Identifier: CA1169462482
Gene: TACSTD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576757G= , CM000663.2:g.58576757G= GRCh38
NC_000001.10:g.59042429G= , CM000663.1:g.59042429G= GRCh37
NC_000001.9:g.58815017G= NCBI36
NG_016237.1:g.5738C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.400C= MANE Select ENSP00000360269.2:p.Arg134=
ENST00000371225.3:c.400C= ENSP00000360269.2:p.Arg134=
NM_002353.2:c.400C= NP_002344.2:p.Arg134=
NM_002353.3:c.400C= MANE Select NP_002344.2:p.Arg134=