Canonical Allele Identifier: CA519928802
Gene: TAB3P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.15272987C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13161076C>G , CM000686.2:g.13161076C>G GRCh38
NC_000024.9:g.15272987C>G , CM000686.1:g.15272987C>G GRCh37
NC_000024.8:g.13782381C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439217.1:n.474G>C
ENST00000452645.1:n.1139G>C
Search 100 bp 5'
Search 100 bp 3'