Canonical Allele Identifier: CA340525892
Gene: TACSTD2 HGNC NCBI

Linked Data

gnomAD v4: 1-58576720-T-C
MyVariant Identifiers: chr1:g.59042392T>C (hg19) chr1:g.58576720T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576720T>C , CM000663.2:g.58576720T>C GRCh38
NC_000001.10:g.59042392T>C , CM000663.1:g.59042392T>C GRCh37
NC_000001.9:g.58814980T>C NCBI36
NG_016237.1:g.5775A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.437A>G MANE Select ENSP00000360269.2:p.Asp146Gly
ENST00000371225.3:c.437A>G ENSP00000360269.2:p.Asp146Gly
NM_002353.2:c.437A>G NP_002344.2:p.Asp146Gly
NM_002353.3:c.437A>G MANE Select NP_002344.2:p.Asp146Gly
Search 100 bp 5'
Search 100 bp 3'