Canonical Allele Identifier: CA10611306
Gene: TACSTD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 297754
ClinVar RCV Id: RCV000355047
dbSNP Id: rs9583
gnomAD v2: 1-59041436-T-C
gnomAD v3: 1-58575764-T-C
gnomAD v4: 1-58575764-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58575764T>C , CM000663.2:g.58575764T>C GRCh38
NC_000001.10:g.59041436T>C , CM000663.1:g.59041436T>C GRCh37
NC_000001.9:g.58814024T>C NCBI36
NG_016237.1:g.6731A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.*421A>G MANE Select ENSP00000360269.2:n.*421A>G
ENST00000371225.3:c.*421A>G ENSP00000360269.2:n.*421A>G
NM_002353.2:c.*421A>G NP_002344.2:n.*421A>G
NM_002353.3:c.*421A>G MANE Select NP_002344.2:n.*421A>G