Canonical Allele Identifier: CA340529368
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs1204078093
gnomAD v2: 1-59042569-C-T
gnomAD v4: 1-58576897-C-T
MyVariant Identifiers: chr1:g.59042569C>T (hg19) chr1:g.58576897C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576897C>T , CM000663.2:g.58576897C>T GRCh38
NC_000001.10:g.59042569C>T , CM000663.1:g.59042569C>T GRCh37
NC_000001.9:g.58815157C>T NCBI36
NG_016237.1:g.5598G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.260G>A MANE Select ENSP00000360269.2:p.Arg87His
ENST00000371225.3:c.260G>A ENSP00000360269.2:p.Arg87His
NM_002353.2:c.260G>A NP_002344.2:p.Arg87His
NM_002353.3:c.260G>A MANE Select NP_002344.2:p.Arg87His
Search 100 bp 5'
Search 100 bp 3'