Canonical Allele Identifier: CA418183090
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs774486053
gnomAD v2: 1-59042559-C-T
MyVariant Identifiers: chr1:g.59042559C>T (hg19) chr1:g.58576887C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576887C>T , CM000663.2:g.58576887C>T GRCh38
NC_000001.10:g.59042559C>T , CM000663.1:g.59042559C>T GRCh37
NC_000001.9:g.58815147C>T NCBI36
NG_016237.1:g.5608G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.270G>A MANE Select ENSP00000360269.2:p.Val90=
ENST00000371225.3:c.270G>A ENSP00000360269.2:p.Val90=
NM_002353.2:c.270G>A NP_002344.2:p.Val90=
NM_002353.3:c.270G>A MANE Select NP_002344.2:p.Val90=
Search 100 bp 5'
Search 100 bp 3'