Canonical Allele Identifier: CA10611306

Gene: TACSTD2

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
• MyVariant Identifiers: chr1:g.59041436T>C (hg19) ; chr1:g.58575764T>C (hg38)

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