Canonical Allele Identifier: CA923767783
Gene: TXLNGY HGNC NCBI

Linked Data

gnomAD v3: Y-19577687-A-T
gnomAD v4: Y-19577687-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19577687A>T , CM000686.2:g.19577687A>T GRCh38
NC_000024.9:g.21739573A>T , CM000686.1:g.21739573A>T GRCh37
NC_000024.8:g.20198961A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.200-9523A>T
ENST00000686905.1:n.134-9523A>T
ENST00000693214.1:n.222-9523A>T
ENST00000445715.6:n.102-9523A>T
ENST00000407724.7:n.171-9523A>T
ENST00000445715.5:n.102-9523A>T
ENST00000447202.2:n.124-9523A>T
ENST00000447520.5:n.102-9523A>T
ENST00000459719.6:n.222-9523A>T
ENST00000538014.2:n.240+8228A>T
NR_045128.1:n.126-9523A>T
NR_045129.1:n.126-9523A>T