Canonical Allele Identifier: CA520139163
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751580T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589694T>A , CM000686.2:g.19589694T>A GRCh38
NC_000024.9:g.21751580T>A , CM000686.1:g.21751580T>A GRCh37
NC_000024.8:g.20210968T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.589+82T>A
ENST00000686905.1:n.1756T>A
ENST00000693214.1:n.1844T>A
ENST00000445715.6:n.491+82T>A
ENST00000407724.7:n.835+82T>A
ENST00000445715.5:n.491+82T>A
ENST00000447202.2:n.2608T>A
ENST00000447520.5:n.491+82T>A
ENST00000459719.6:n.1762+82T>A
ENST00000538014.2:n.1863T>A
ENST00000585549.5:n.134+82T>A
ENST00000587095.1:n.132+82T>A
ENST00000588613.5:n.200+82T>A
ENST00000589075.5:n.173+82T>A
NR_045128.1:n.515+82T>A
NR_045129.1:n.515+82T>A
Search 100 bp 5'
Search 100 bp 3'