Canonical Allele Identifier: CA340526668

Gene: TACSTD2

Linked Data

• MyVariant Identifiers: chr1:g.59042466C>A (hg19) ; chr1:g.58576794C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58576794C>A , CM000663.2:g.58576794C>A	GRCh38
NC_000001.10:g.59042466C>A , CM000663.1:g.59042466C>A	GRCh37
NC_000001.9:g.58815054C>A	NCBI36
NG_016237.1:g.5701G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.363G>T MANE Select	ENSP00000360269.2:p.Gln121His
ENST00000371225.3:c.363G>T	ENSP00000360269.2:p.Gln121His
NM_002353.2:c.363G>T	NP_002344.2:p.Gln121His
NM_002353.3:c.363G>T MANE Select	NP_002344.2:p.Gln121His