Canonical Allele Identifier: CA418182920
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs1185027530
gnomAD v2: 1-59042448-G-A
gnomAD v4: 1-58576776-G-A
MyVariant Identifiers: chr1:g.59042448G>A (hg19) chr1:g.58576776G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576776G>A , CM000663.2:g.58576776G>A GRCh38
NC_000001.10:g.59042448G>A , CM000663.1:g.59042448G>A GRCh37
NC_000001.9:g.58815036G>A NCBI36
NG_016237.1:g.5719C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.381C>T MANE Select ENSP00000360269.2:p.Cys127=
ENST00000371225.3:c.381C>T ENSP00000360269.2:p.Cys127=
NM_002353.2:c.381C>T NP_002344.2:p.Cys127=
NM_002353.3:c.381C>T MANE Select NP_002344.2:p.Cys127=
Search 100 bp 5'
Search 100 bp 3'