Canonical Allele Identifier: CA10611439

Gene: TACSTD2

Linked Data

• ClinVar Variation Id: 297779
• ClinVar RCV Id: RCV000327661
• dbSNP Id: rs886046458
• gnomAD v3: 1-58577425-C-G
• gnomAD v4: 1-58577425-C-G
• MyVariant Identifiers: chr1:g.59043097C>G (hg19) ; chr1:g.58577425C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58577425C>G , CM000663.2:g.58577425C>G	GRCh38
NC_000001.10:g.59043097C>G , CM000663.1:g.59043097C>G	GRCh37
NC_000001.9:g.58815685C>G	NCBI36
NG_016237.1:g.5070G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.3:c.-269G>C	ENSP00000360269.2:n.-269G>C
NM_002353.2:c.-269G>C	NP_002344.2:n.-269G>C