Canonical Allele Identifier: CA22878522
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs764259617
MyVariant Identifiers: chr1:g.59042431A>C (hg19) chr1:g.58576759A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576759A>C , CM000663.2:g.58576759A>C GRCh38
NC_000001.10:g.59042431A>C , CM000663.1:g.59042431A>C GRCh37
NC_000001.9:g.58815019A>C NCBI36
NG_016237.1:g.5736T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.398T>G MANE Select ENSP00000360269.2:p.Val133Gly
ENST00000371225.3:c.398T>G ENSP00000360269.2:p.Val133Gly
NM_002353.2:c.398T>G NP_002344.2:p.Val133Gly
NM_002353.3:c.398T>G MANE Select NP_002344.2:p.Val133Gly
Search 100 bp 5'
Search 100 bp 3'