Canonical Allele Identifier: CA880362157
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs1374611240

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19568311A>G , CM000686.2:g.19568311A>G GRCh38
NC_000024.9:g.21730197A>G , CM000686.1:g.21730197A>G GRCh37
NC_000024.8:g.20189585A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000685919.1:n.960A>G
ENST00000686158.1:n.199+741A>G
ENST00000686905.1:n.133+829A>G
ENST00000688167.1:n.960A>G
ENST00000688449.1:n.473A>G
ENST00000689102.1:n.481A>G
ENST00000691331.1:n.481A>G
ENST00000691759.1:n.473A>G
ENST00000693214.1:n.221+741A>G
ENST00000445715.6:n.101+829A>G
ENST00000407724.7:n.170+829A>G
ENST00000445715.5:n.101+829A>G
ENST00000447202.2:n.123+360A>G
ENST00000447520.5:n.101+829A>G
ENST00000459719.6:n.221+741A>G
ENST00000538014.2:n.165+360A>G
NR_045128.1:n.125+829A>G
NR_045129.1:n.125+829A>G