Canonical Allele Identifier: CA340524409
Gene: TACSTD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2245199
ClinVar RCV Id: RCV002732746
dbSNP Id: rs1208621599
gnomAD v2: 1-59042220-G-C
gnomAD v3: 1-58576548-G-C
gnomAD v4: 1-58576548-G-C
MyVariant Identifiers: chr1:g.59042220G>C (hg19) chr1:g.58576548G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576548G>C , CM000663.2:g.58576548G>C GRCh38
NC_000001.10:g.59042220G>C , CM000663.1:g.59042220G>C GRCh37
NC_000001.9:g.58814808G>C NCBI36
NG_016237.1:g.5947C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371225.4:c.609C>G MANE Select ENSP00000360269.2:p.Ile203Met
ENST00000371225.3:c.609C>G ENSP00000360269.2:p.Ile203Met
NM_002353.2:c.609C>G NP_002344.2:p.Ile203Met
NM_002353.3:c.609C>G MANE Select NP_002344.2:p.Ile203Met
Search 100 bp 5'
Search 100 bp 3'