Canonical Allele Identifier: CA2470909235
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs1603544193

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19568322A>G , CM000686.2:g.19568322A>G GRCh38
NC_000024.9:g.21730208A>G , CM000686.1:g.21730208A>G GRCh37
NC_000024.8:g.20189596A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000685919.1:n.971A>G
ENST00000686158.1:n.199+752A>G
ENST00000686905.1:n.133+840A>G
ENST00000688167.1:n.971A>G
ENST00000688449.1:n.484A>G
ENST00000689102.1:n.492A>G
ENST00000691331.1:n.492A>G
ENST00000691759.1:n.484A>G
ENST00000693214.1:n.221+752A>G
ENST00000445715.6:n.101+840A>G
ENST00000407724.7:n.170+840A>G
ENST00000445715.5:n.101+840A>G
ENST00000447202.2:n.123+371A>G
ENST00000447520.5:n.101+840A>G
ENST00000459719.6:n.221+752A>G
ENST00000538014.2:n.165+371A>G
NR_045128.1:n.125+840A>G
NR_045129.1:n.125+840A>G