Canonical Allele Identifier: CA880362260
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs1484614024

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19577774G>A , CM000686.2:g.19577774G>A GRCh38
NC_000024.9:g.21739660G>A , CM000686.1:g.21739660G>A GRCh37
NC_000024.8:g.20199048G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.200-9436G>A
ENST00000686905.1:n.134-9436G>A
ENST00000693214.1:n.222-9436G>A
ENST00000445715.6:n.102-9436G>A
ENST00000407724.7:n.171-9436G>A
ENST00000445715.5:n.102-9436G>A
ENST00000447202.2:n.124-9436G>A
ENST00000447520.5:n.102-9436G>A
ENST00000459719.6:n.222-9436G>A
ENST00000538014.2:n.240+8315G>A
NR_045128.1:n.126-9436G>A
NR_045129.1:n.126-9436G>A