Canonical Allele Identifier: CA340527360
Gene: TACSTD2 HGNC NCBI

Linked Data

gnomAD v4: 1-58576850-G-T
MyVariant Identifiers: chr1:g.59042522G>T (hg19) chr1:g.58576850G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576850G>T , CM000663.2:g.58576850G>T GRCh38
NC_000001.10:g.59042522G>T , CM000663.1:g.59042522G>T GRCh37
NC_000001.9:g.58815110G>T NCBI36
NG_016237.1:g.5645C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.307C>A MANE Select ENSP00000360269.2:p.Leu103Ile
ENST00000371225.3:c.307C>A ENSP00000360269.2:p.Leu103Ile
NM_002353.2:c.307C>A NP_002344.2:p.Leu103Ile
NM_002353.3:c.307C>A MANE Select NP_002344.2:p.Leu103Ile
Search 100 bp 5'
Search 100 bp 3'