Canonical Allele Identifier: CA337400727
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs796260123

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19602572A>G , CM000686.2:g.19602572A>G GRCh38
NC_000024.9:g.21764458A>G , CM000686.1:g.21764458A>G GRCh37
NC_000024.8:g.20223846A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000445715.6:n.1250+261A>G
ENST00000253320.8:n.4821+261A>G
ENST00000445715.5:n.1591+261A>G
ENST00000592697.1:n.586+261A>G
NR_045128.1:n.1274+261A>G