Canonical Allele Identifier: CA337400905
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs111725135
gnomAD v3: Y-19606073-C-T
gnomAD v4: Y-19606073-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19606073C>T , CM000686.2:g.19606073C>T GRCh38
NC_000024.9:g.21767959C>T , CM000686.1:g.21767959C>T GRCh37
NC_000024.8:g.20227347C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000253320.8:n.7098C>T
NR_045128.1:n.3551C>T