Canonical Allele Identifier: CA923764239

Gene: TXLNGY

Linked Data

• dbSNP Id: rs2045116115
• gnomAD v3: Y-19568362-T-C
• gnomAD v4: Y-19568362-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19568362T>C , CM000686.2:g.19568362T>C	GRCh38
NC_000024.9:g.21730248T>C , CM000686.1:g.21730248T>C	GRCh37
NC_000024.8:g.20189636T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685919.1:n.1011T>C
ENST00000686158.1:n.199+792T>C
ENST00000686905.1:n.133+880T>C
ENST00000688167.1:n.1011T>C
ENST00000688449.1:n.524T>C
ENST00000689102.1:n.532T>C
ENST00000691331.1:n.532T>C
ENST00000691759.1:n.524T>C
ENST00000693214.1:n.221+792T>C
ENST00000445715.6:n.101+880T>C
ENST00000407724.7:n.170+880T>C
ENST00000445715.5:n.101+880T>C
ENST00000447202.2:n.123+411T>C
ENST00000447520.5:n.101+880T>C
ENST00000459719.6:n.221+792T>C
ENST00000538014.2:n.165+411T>C
NR_045128.1:n.125+880T>C
NR_045129.1:n.125+880T>C