Canonical Allele Identifier: CA340523814
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs1297690032
gnomAD v2: 1-59042111-C-A
gnomAD v4: 1-58576439-C-A
MyVariant Identifiers: chr1:g.59042111C>A (hg19) chr1:g.58576439C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576439C>A , CM000663.2:g.58576439C>A GRCh38
NC_000001.10:g.59042111C>A , CM000663.1:g.59042111C>A GRCh37
NC_000001.9:g.58814699C>A NCBI36
NG_016237.1:g.6056G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371225.4:c.718G>T MANE Select ENSP00000360269.2:p.Gly240Cys
ENST00000371225.3:c.718G>T ENSP00000360269.2:p.Gly240Cys
NM_002353.2:c.718G>T NP_002344.2:p.Gly240Cys
NM_002353.3:c.718G>T MANE Select NP_002344.2:p.Gly240Cys
Search 100 bp 5'
Search 100 bp 3'