Canonical Allele Identifier: CA337399308

Gene: TXLNGY

Linked Data

• dbSNP Id: rs999129533
• MyVariant Identifiers: chrY:g.21730204T>G (hg19) ; chrY:g.19568318T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19568318T>G , CM000686.2:g.19568318T>G	GRCh38
NC_000024.9:g.21730204T>G , CM000686.1:g.21730204T>G	GRCh37
NC_000024.8:g.20189592T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685919.1:n.967T>G
ENST00000686158.1:n.199+748T>G
ENST00000686905.1:n.133+836T>G
ENST00000688167.1:n.967T>G
ENST00000688449.1:n.480T>G
ENST00000689102.1:n.488T>G
ENST00000691331.1:n.488T>G
ENST00000691759.1:n.480T>G
ENST00000693214.1:n.221+748T>G
ENST00000445715.6:n.101+836T>G
ENST00000407724.7:n.170+836T>G
ENST00000445715.5:n.101+836T>G
ENST00000447202.2:n.123+367T>G
ENST00000447520.5:n.101+836T>G
ENST00000459719.6:n.221+748T>G
ENST00000538014.2:n.165+367T>G
NR_045128.1:n.125+836T>G
NR_045129.1:n.125+836T>G