Canonical Allele Identifier: CA923765180
Gene: TXLNGY HGNC NCBI

Linked Data

gnomAD v3: Y-19570465-C-T
gnomAD v4: Y-19570465-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19570465C>T , CM000686.2:g.19570465C>T GRCh38
NC_000024.9:g.21732351C>T , CM000686.1:g.21732351C>T GRCh37
NC_000024.8:g.20191739C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.199+2895C>T
ENST00000686905.1:n.133+2983C>T
ENST00000693214.1:n.221+2895C>T
ENST00000445715.6:n.101+2983C>T
ENST00000407724.7:n.170+2983C>T
ENST00000445715.5:n.101+2983C>T
ENST00000447202.2:n.123+2514C>T
ENST00000447520.5:n.101+2983C>T
ENST00000459719.6:n.221+2895C>T
ENST00000538014.2:n.240+1006C>T
NR_045128.1:n.125+2983C>T
NR_045129.1:n.125+2983C>T