Canonical Allele Identifier: CA337399652
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs749221926
gnomAD v3: Y-19577740-C-T
gnomAD v4: Y-19577740-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19577740C>T , CM000686.2:g.19577740C>T GRCh38
NC_000024.9:g.21739626C>T , CM000686.1:g.21739626C>T GRCh37
NC_000024.8:g.20199014C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.200-9470C>T
ENST00000686905.1:n.134-9470C>T
ENST00000693214.1:n.222-9470C>T
ENST00000445715.6:n.102-9470C>T
ENST00000407724.7:n.171-9470C>T
ENST00000445715.5:n.102-9470C>T
ENST00000447202.2:n.124-9470C>T
ENST00000447520.5:n.102-9470C>T
ENST00000459719.6:n.222-9470C>T
ENST00000538014.2:n.240+8281C>T
NR_045128.1:n.126-9470C>T
NR_045129.1:n.126-9470C>T