Canonical Allele Identifier: CA337400288
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs796727509

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589665C>T , CM000686.2:g.19589665C>T GRCh38
NC_000024.9:g.21751551C>T , CM000686.1:g.21751551C>T GRCh37
NC_000024.8:g.20210939C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.589+53C>T
ENST00000686905.1:n.1727C>T
ENST00000693214.1:n.1815C>T
ENST00000445715.6:n.491+53C>T
ENST00000407724.7:n.835+53C>T
ENST00000445715.5:n.491+53C>T
ENST00000447202.2:n.2579C>T
ENST00000447520.5:n.491+53C>T
ENST00000459719.6:n.1762+53C>T
ENST00000538014.2:n.1834C>T
ENST00000585549.5:n.134+53C>T
ENST00000587095.1:n.132+53C>T
ENST00000588613.5:n.200+53C>T
ENST00000589075.5:n.173+53C>T
NR_045128.1:n.515+53C>T
NR_045129.1:n.515+53C>T