Canonical Allele Identifier: CA418182929
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs766747165
gnomAD v2: 1-59042460-C-A
gnomAD v3: 1-58576788-C-A
gnomAD v4: 1-58576788-C-A
MyVariant Identifiers: chr1:g.59042460C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576788C>A , CM000663.2:g.58576788C>A GRCh38
NC_000001.10:g.59042460C>A , CM000663.1:g.59042460C>A GRCh37
NC_000001.9:g.58815048C>A NCBI36
NG_016237.1:g.5707G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.369G>T MANE Select ENSP00000360269.2:p.Ser123=
ENST00000371225.3:c.369G>T ENSP00000360269.2:p.Ser123=
NM_002353.2:c.369G>T NP_002344.2:p.Ser123=
NM_002353.3:c.369G>T MANE Select NP_002344.2:p.Ser123=
Search 100 bp 5'
Search 100 bp 3'