Canonical Allele Identifier: CA2838305362
Gene: TLX1NB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101124865T>C , CM000672.2:g.101124865T>C GRCh38
NC_000010.10:g.102884622T>C , CM000672.1:g.102884622T>C GRCh37
NC_000010.9:g.102874612T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130722.1:n.529+2095A>G
NR_130723.1:n.500+2095A>G
NR_130724.1:n.718+2095A>G