Canonical Allele Identifier: CA337399658

Gene: TXLNGY

Linked Data

• dbSNP Id: rs376303746
• gnomAD v3: Y-19577760-C-G
• gnomAD v4: Y-19577760-C-G
• MyVariant Identifiers: chrY:g.21739646C>G (hg19) ; chrY:g.19577760C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19577760C>G , CM000686.2:g.19577760C>G	GRCh38
NC_000024.9:g.21739646C>G , CM000686.1:g.21739646C>G	GRCh37
NC_000024.8:g.20199034C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.200-9450C>G
ENST00000686905.1:n.134-9450C>G
ENST00000693214.1:n.222-9450C>G
ENST00000445715.6:n.102-9450C>G
ENST00000407724.7:n.171-9450C>G
ENST00000445715.5:n.102-9450C>G
ENST00000447202.2:n.124-9450C>G
ENST00000447520.5:n.102-9450C>G
ENST00000459719.6:n.222-9450C>G
ENST00000538014.2:n.240+8301C>G
NR_045128.1:n.126-9450C>G
NR_045129.1:n.126-9450C>G