Canonical Allele Identifier: CA340527912

Gene: TACSTD2

Linked Data

• dbSNP Id: rs1388416037
• gnomAD v2: 1-59042555-G-A
• gnomAD v4: 1-58576883-G-A
• MyVariant Identifiers: chr1:g.59042555G>A (hg19) ; chr1:g.58576883G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58576883G>A , CM000663.2:g.58576883G>A	GRCh38
NC_000001.10:g.59042555G>A , CM000663.1:g.59042555G>A	GRCh37
NC_000001.9:g.58815143G>A	NCBI36
NG_016237.1:g.5612C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.274C>T MANE Select	ENSP00000360269.2:p.Pro92Ser
ENST00000371225.3:c.274C>T	ENSP00000360269.2:p.Pro92Ser
NM_002353.2:c.274C>T	NP_002344.2:p.Pro92Ser
NM_002353.3:c.274C>T MANE Select	NP_002344.2:p.Pro92Ser