Canonical Allele Identifier: CA923765186
Gene: TXLNGY HGNC NCBI

Linked Data

gnomAD v3: Y-19570500-A-G
gnomAD v4: Y-19570500-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19570500A>G , CM000686.2:g.19570500A>G GRCh38
NC_000024.9:g.21732386A>G , CM000686.1:g.21732386A>G GRCh37
NC_000024.8:g.20191774A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.199+2930A>G
ENST00000686905.1:n.133+3018A>G
ENST00000693214.1:n.221+2930A>G
ENST00000445715.6:n.101+3018A>G
ENST00000407724.7:n.170+3018A>G
ENST00000445715.5:n.101+3018A>G
ENST00000447202.2:n.123+2549A>G
ENST00000447520.5:n.101+3018A>G
ENST00000459719.6:n.221+2930A>G
ENST00000538014.2:n.240+1041A>G
NR_045128.1:n.125+3018A>G
NR_045129.1:n.125+3018A>G