Canonical Allele Identifier: CA10610207

Gene: TACSTD2

Linked Data

• ClinVar Variation Id: 297759
• ClinVar RCV Id: RCV000323278
• dbSNP Id: rs7355042
• gnomAD v2: 1-59041691-G-A
• gnomAD v3: 1-58576019-G-A
• gnomAD v4: 1-58576019-G-A
• MyVariant Identifiers: chr1:g.59041691G>A (hg19) ; chr1:g.58576019G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58576019G>A , CM000663.2:g.58576019G>A	GRCh38
NC_000001.10:g.59041691G>A , CM000663.1:g.59041691G>A	GRCh37
NC_000001.9:g.58814279G>A	NCBI36
NG_016237.1:g.6476C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.*166C>T MANE Select	ENSP00000360269.2:n.*166C>T
ENST00000371225.3:c.*166C>T	ENSP00000360269.2:n.*166C>T
NM_002353.2:c.*166C>T	NP_002344.2:n.*166C>T
NM_002353.3:c.*166C>T MANE Select	NP_002344.2:n.*166C>T