Canonical Allele Identifier: CA340526302

Gene: TACSTD2

Linked Data

• gnomAD v4: 1-58576763-C-G
• MyVariant Identifiers: chr1:g.59042435C>G (hg19) ; chr1:g.58576763C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.58576763C>G , CM000663.2:g.58576763C>G	GRCh38
NC_000001.10:g.59042435C>G , CM000663.1:g.59042435C>G	GRCh37
NC_000001.9:g.58815023C>G	NCBI36
NG_016237.1:g.5732G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371225.4:c.394G>C MANE Select	ENSP00000360269.2:p.Gly132Arg
ENST00000371225.3:c.394G>C	ENSP00000360269.2:p.Gly132Arg
NM_002353.2:c.394G>C	NP_002344.2:p.Gly132Arg
NM_002353.3:c.394G>C MANE Select	NP_002344.2:p.Gly132Arg