Canonical Allele Identifier: CA337399527
Gene: TXLNGY HGNC NCBI

Linked Data

dbSNP Id: rs890685078
gnomAD v3: Y-19574440-C-T
gnomAD v4: Y-19574440-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19574440C>T , CM000686.2:g.19574440C>T GRCh38
NC_000024.9:g.21736326C>T , CM000686.1:g.21736326C>T GRCh37
NC_000024.8:g.20195714C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.199+6870C>T
ENST00000686905.1:n.133+6958C>T
ENST00000693214.1:n.221+6870C>T
ENST00000445715.6:n.101+6958C>T
ENST00000407724.7:n.170+6958C>T
ENST00000445715.5:n.101+6958C>T
ENST00000447202.2:n.123+6489C>T
ENST00000447520.5:n.101+6958C>T
ENST00000459719.6:n.221+6870C>T
ENST00000538014.2:n.240+4981C>T
NR_045128.1:n.125+6958C>T
NR_045129.1:n.125+6958C>T