Canonical Allele Identifier: CA2470911119
Gene: TXLNGY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19602614C= , CM000686.2:g.19602614C= GRCh38
NC_000024.9:g.21764500C= , CM000686.1:g.21764500C= GRCh37
NC_000024.8:g.20223888C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_045128.1:n.1274+303C=
ENST00000253320.8:n.4821+303C=
ENST00000445715.5:n.1591+303C=
ENST00000445715.6:n.1250+303C=
ENST00000592697.1:n.586+303C=