Canonical Allele Identifier: CA418183064
Gene: TACSTD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59042553C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576881C>G , CM000663.2:g.58576881C>G GRCh38
NC_000001.10:g.59042553C>G , CM000663.1:g.59042553C>G GRCh37
NC_000001.9:g.58815141C>G NCBI36
NG_016237.1:g.5614G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.276G>C MANE Select ENSP00000360269.2:p.Pro92=
ENST00000371225.3:c.276G>C ENSP00000360269.2:p.Pro92=
NM_002353.2:c.276G>C NP_002344.2:p.Pro92=
NM_002353.3:c.276G>C MANE Select NP_002344.2:p.Pro92=