Canonical Allele Identifier: CA520137014
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751351G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589465G>A , CM000686.2:g.19589465G>A GRCh38
NC_000024.9:g.21751351G>A , CM000686.1:g.21751351G>A GRCh37
NC_000024.8:g.20210739G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.498-56G>A
ENST00000686905.1:n.1527G>A
ENST00000693214.1:n.1615G>A
ENST00000445715.6:n.400-56G>A
ENST00000407724.7:n.750-62G>A
ENST00000445715.5:n.400-56G>A
ENST00000447202.2:n.2379G>A
ENST00000447520.5:n.400-56G>A
ENST00000459719.6:n.1615G>A
ENST00000538014.2:n.1634G>A
ENST00000585549.5:n.43-56G>A
ENST00000587095.1:n.41-56G>A
ENST00000588613.5:n.109-56G>A
ENST00000589075.5:n.82-56G>A
NR_045128.1:n.424-56G>A
NR_045129.1:n.424-56G>A