Canonical Allele Identifier: CA418182913
Gene: TACSTD2 HGNC NCBI

Linked Data

gnomAD v4: 1-58576770-G-A
MyVariant Identifiers: chr1:g.59042442G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576770G>A , CM000663.2:g.58576770G>A GRCh38
NC_000001.10:g.59042442G>A , CM000663.1:g.59042442G>A GRCh37
NC_000001.9:g.58815030G>A NCBI36
NG_016237.1:g.5725C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.387C>T MANE Select ENSP00000360269.2:p.Asn129=
ENST00000371225.3:c.387C>T ENSP00000360269.2:p.Asn129=
NM_002353.2:c.387C>T NP_002344.2:p.Asn129=
NM_002353.3:c.387C>T MANE Select NP_002344.2:p.Asn129=
Search 100 bp 5'
Search 100 bp 3'