Canonical Allele Identifier: CA520140387

Gene: TXLNGY

Linked Data

• dbSNP Id: rs1603544404
• MyVariant Identifiers: chrY:g.21751707A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589821A>T , CM000686.2:g.19589821A>T	GRCh38
NC_000024.9:g.21751707A>T , CM000686.1:g.21751707A>T	GRCh37
NC_000024.8:g.20211095A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.589+209A>T
ENST00000686905.1:n.1883A>T
ENST00000693214.1:n.1971A>T
ENST00000445715.6:n.491+209A>T
ENST00000407724.7:n.835+209A>T
ENST00000445715.5:n.491+209A>T
ENST00000447202.2:n.2735A>T
ENST00000447520.5:n.491+209A>T
ENST00000459719.6:n.1762+209A>T
ENST00000538014.2:n.1990A>T
ENST00000585549.5:n.134+209A>T
ENST00000587095.1:n.132+209A>T
ENST00000588613.5:n.200+209A>T
ENST00000589075.5:n.173+209A>T
NR_045128.1:n.515+209A>T
NR_045129.1:n.515+209A>T