Canonical Allele Identifier: CA418183065
Gene: TACSTD2 HGNC NCBI

Linked Data

dbSNP Id: rs1371351104
gnomAD v2: 1-59042553-C-T
gnomAD v4: 1-58576881-C-T
MyVariant Identifiers: chr1:g.59042553C>T (hg19) chr1:g.58576881C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576881C>T , CM000663.2:g.58576881C>T GRCh38
NC_000001.10:g.59042553C>T , CM000663.1:g.59042553C>T GRCh37
NC_000001.9:g.58815141C>T NCBI36
NG_016237.1:g.5614G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.276G>A MANE Select ENSP00000360269.2:p.Pro92=
ENST00000371225.3:c.276G>A ENSP00000360269.2:p.Pro92=
NM_002353.2:c.276G>A NP_002344.2:p.Pro92=
NM_002353.3:c.276G>A MANE Select NP_002344.2:p.Pro92=
Search 100 bp 5'
Search 100 bp 3'