Canonical Allele Identifier: CA2470911115
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs1603544452

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19602571T>C , CM000686.2:g.19602571T>C GRCh38
NC_000024.9:g.21764457T>C , CM000686.1:g.21764457T>C GRCh37
NC_000024.8:g.20223845T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000445715.6:n.1250+260T>C
ENST00000253320.8:n.4821+260T>C
ENST00000445715.5:n.1591+260T>C
ENST00000592697.1:n.586+260T>C
NR_045128.1:n.1274+260T>C