Canonical Allele Identifier: CA337400733
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs13447370
gnomAD v3: Y-19602614-C-T
gnomAD v4: Y-19602614-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19602614C>T , CM000686.2:g.19602614C>T GRCh38
NC_000024.9:g.21764500C>T , CM000686.1:g.21764500C>T GRCh37
NC_000024.8:g.20223888C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000445715.6:n.1250+303C>T
ENST00000253320.8:n.4821+303C>T
ENST00000445715.5:n.1591+303C>T
ENST00000592697.1:n.586+303C>T
NR_045128.1:n.1274+303C>T