Canonical Allele Identifier: CA923766363
Gene: TXLNGY HGNC NCBI

Linked Data

gnomAD v3: Y-19574312-G-T
gnomAD v4: Y-19574312-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19574312G>T , CM000686.2:g.19574312G>T GRCh38
NC_000024.9:g.21736198G>T , CM000686.1:g.21736198G>T GRCh37
NC_000024.8:g.20195586G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.199+6742G>T
ENST00000686905.1:n.133+6830G>T
ENST00000693214.1:n.221+6742G>T
ENST00000445715.6:n.101+6830G>T
ENST00000407724.7:n.170+6830G>T
ENST00000445715.5:n.101+6830G>T
ENST00000447202.2:n.123+6361G>T
ENST00000447520.5:n.101+6830G>T
ENST00000459719.6:n.221+6742G>T
ENST00000538014.2:n.240+4853G>T
NR_045128.1:n.125+6830G>T
NR_045129.1:n.125+6830G>T
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