Canonical Allele Identifier: CA519928793
Gene: TAB3P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.15272984G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13161073G>C , CM000686.2:g.13161073G>C GRCh38
NC_000024.9:g.15272984G>C , CM000686.1:g.15272984G>C GRCh37
NC_000024.8:g.13782378G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439217.1:n.477C>G
ENST00000452645.1:n.1142C>G