Canonical Allele Identifier: CA337399313

Gene: TXLNGY

Linked Data

• dbSNP Id: rs893065019
• MyVariant Identifiers: chrY:g.21730365A>G (hg19) ; chrY:g.19568479A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19568479A>G , CM000686.2:g.19568479A>G	GRCh38
NC_000024.9:g.21730365A>G , CM000686.1:g.21730365A>G	GRCh37
NC_000024.8:g.20189753A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685919.1:n.1128A>G
ENST00000686158.1:n.199+909A>G
ENST00000686905.1:n.133+997A>G
ENST00000688167.1:n.1128A>G
ENST00000688449.1:n.641A>G
ENST00000689102.1:n.649A>G
ENST00000691331.1:n.649A>G
ENST00000691759.1:n.641A>G
ENST00000693214.1:n.221+909A>G
ENST00000445715.6:n.101+997A>G
ENST00000407724.7:n.170+997A>G
ENST00000445715.5:n.101+997A>G
ENST00000447202.2:n.123+528A>G
ENST00000447520.5:n.101+997A>G
ENST00000459719.6:n.221+909A>G
ENST00000538014.2:n.165+528A>G
NR_045128.1:n.125+997A>G
NR_045129.1:n.125+997A>G