Canonical Allele Identifier: CA877430
Gene: TACSTD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3173362
ClinVar RCV Id: RCV004466268
dbSNP Id: rs144588105
ExAC: 1:59042404 C / T
gnomAD v2: 1-59042404-C-T
gnomAD v4: 1-58576732-C-T
MyVariant Identifiers: chr1:g.59042404C>T (hg19) chr1:g.58576732C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576732C>T , CM000663.2:g.58576732C>T GRCh38
NC_000001.10:g.59042404C>T , CM000663.1:g.59042404C>T GRCh37
NC_000001.9:g.58814992C>T NCBI36
NG_016237.1:g.5763G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.425G>A MANE Select ENSP00000360269.2:p.Ser142Asn
ENST00000371225.3:c.425G>A ENSP00000360269.2:p.Ser142Asn
NM_002353.2:c.425G>A NP_002344.2:p.Ser142Asn
NM_002353.3:c.425G>A MANE Select NP_002344.2:p.Ser142Asn
Search 100 bp 5'
Search 100 bp 3'