Canonical Allele Identifier: CA2470910545
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs1603544406
gnomAD v4: Y-19589878-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589878G>T , CM000686.2:g.19589878G>T GRCh38
NC_000024.9:g.21751764G>T , CM000686.1:g.21751764G>T GRCh37
NC_000024.8:g.20211152G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.590-205G>T
ENST00000693214.1:n.2028G>T
ENST00000445715.6:n.491+266G>T
ENST00000407724.7:n.836-205G>T
ENST00000445715.5:n.492-205G>T
ENST00000447520.5:n.492-205G>T
ENST00000459719.6:n.1763-205G>T
ENST00000585549.5:n.134+266G>T
ENST00000587095.1:n.132+266G>T
ENST00000588613.5:n.200+266G>T
ENST00000589075.5:n.174-205G>T
NR_045128.1:n.515+266G>T
NR_045129.1:n.516-205G>T