Canonical Allele Identifier: CA519928792
Gene: TAB3P1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.15272984G>A (hg19)
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Genomic Alleles

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

Transcript Alleles

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