Canonical Allele Identifier: CA1619393797
Gene: TNXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32009149C= , CM000668.2:g.32009149C= GRCh38
NC_000006.11:g.31976926C= , CM000668.1:g.31976926C= GRCh37
NC_000006.10:g.32084904C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_001284.2:n.2374G=
ENST00000507684.1:n.1823G=