Canonical Allele Identifier: CA340526814
Gene: TACSTD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.59042480G>C (hg19) chr1:g.58576808G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576808G>C , CM000663.2:g.58576808G>C GRCh38
NC_000001.10:g.59042480G>C , CM000663.1:g.59042480G>C GRCh37
NC_000001.9:g.58815068G>C NCBI36
NG_016237.1:g.5687C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.349C>G MANE Select ENSP00000360269.2:p.Arg117Gly
ENST00000371225.3:c.349C>G ENSP00000360269.2:p.Arg117Gly
NM_002353.2:c.349C>G NP_002344.2:p.Arg117Gly
NM_002353.3:c.349C>G MANE Select NP_002344.2:p.Arg117Gly
Search 100 bp 5'
Search 100 bp 3'