Canonical Allele Identifier: CA1169462328
Gene: TACSTD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576448G= , CM000663.2:g.58576448G= GRCh38
NC_000001.10:g.59042120G= , CM000663.1:g.59042120G= GRCh37
NC_000001.9:g.58814708G= NCBI36
NG_016237.1:g.6047C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371225.4:c.709C= MANE Select ENSP00000360269.2:p.Gln237=
ENST00000371225.3:c.709C= ENSP00000360269.2:p.Gln237=
NM_002353.2:c.709C= NP_002344.2:p.Gln237=
NM_002353.3:c.709C= MANE Select NP_002344.2:p.Gln237=