Canonical Allele Identifier: CA337399533

Gene: TXLNGY

Linked Data

• dbSNP Id: rs796085922
• gnomAD v3: Y-19574445-G-A
• gnomAD v4: Y-19574445-G-A
• MyVariant Identifiers: chrY:g.21736331G>A (hg19) ; chrY:g.19574445G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19574445G>A , CM000686.2:g.19574445G>A	GRCh38
NC_000024.9:g.21736331G>A , CM000686.1:g.21736331G>A	GRCh37
NC_000024.8:g.20195719G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000686158.1:n.199+6875G>A
ENST00000686905.1:n.133+6963G>A
ENST00000693214.1:n.221+6875G>A
ENST00000445715.6:n.101+6963G>A
ENST00000407724.7:n.170+6963G>A
ENST00000445715.5:n.101+6963G>A
ENST00000447202.2:n.123+6494G>A
ENST00000447520.5:n.101+6963G>A
ENST00000459719.6:n.221+6875G>A
ENST00000538014.2:n.240+4986G>A
NR_045128.1:n.125+6963G>A
NR_045129.1:n.125+6963G>A