Canonical Allele Identifier: CA337399312

Gene: TXLNGY

Linked Data

• dbSNP Id: rs386419964
• MyVariant Identifiers: chrY:g.21730357A>C (hg19) ; chrY:g.19568471A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19568471A>C , CM000686.2:g.19568471A>C	GRCh38
NC_000024.9:g.21730357A>C , CM000686.1:g.21730357A>C	GRCh37
NC_000024.8:g.20189745A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685919.1:n.1120A>C
ENST00000686158.1:n.199+901A>C
ENST00000686905.1:n.133+989A>C
ENST00000688167.1:n.1120A>C
ENST00000688449.1:n.633A>C
ENST00000689102.1:n.641A>C
ENST00000691331.1:n.641A>C
ENST00000691759.1:n.633A>C
ENST00000693214.1:n.221+901A>C
ENST00000445715.6:n.101+989A>C
ENST00000407724.7:n.170+989A>C
ENST00000445715.5:n.101+989A>C
ENST00000447202.2:n.123+520A>C
ENST00000447520.5:n.101+989A>C
ENST00000459719.6:n.221+901A>C
ENST00000538014.2:n.165+520A>C
NR_045128.1:n.125+989A>C
NR_045129.1:n.125+989A>C