Canonical Allele Identifier: CA923764230
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs2045116100
gnomAD v3: Y-19568343-G-T
gnomAD v4: Y-19568343-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19568343G>T , CM000686.2:g.19568343G>T GRCh38
NC_000024.9:g.21730229G>T , CM000686.1:g.21730229G>T GRCh37
NC_000024.8:g.20189617G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685919.1:n.992G>T
ENST00000686158.1:n.199+773G>T
ENST00000686905.1:n.133+861G>T
ENST00000688167.1:n.992G>T
ENST00000688449.1:n.505G>T
ENST00000689102.1:n.513G>T
ENST00000691331.1:n.513G>T
ENST00000691759.1:n.505G>T
ENST00000693214.1:n.221+773G>T
ENST00000445715.6:n.101+861G>T
ENST00000407724.7:n.170+861G>T
ENST00000445715.5:n.101+861G>T
ENST00000447202.2:n.123+392G>T
ENST00000447520.5:n.101+861G>T
ENST00000459719.6:n.221+773G>T
ENST00000538014.2:n.165+392G>T
NR_045128.1:n.125+861G>T
NR_045129.1:n.125+861G>T