Canonical Allele Identifier: CA337400273

Gene: TXLNGY

Linked Data

• dbSNP Id: rs201771294
• MyVariant Identifiers: chrY:g.21751450G>A (hg19) ; chrY:g.19589564G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589564G>A , CM000686.2:g.19589564G>A	GRCh38
NC_000024.9:g.21751450G>A , CM000686.1:g.21751450G>A	GRCh37
NC_000024.8:g.20210838G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686158.1:n.541G>A
ENST00000686905.1:n.1626G>A
ENST00000693214.1:n.1714G>A
ENST00000445715.6:n.443G>A
ENST00000407724.7:n.787G>A
ENST00000445715.5:n.443G>A
ENST00000447202.2:n.2478G>A
ENST00000447520.5:n.443G>A
ENST00000459719.6:n.1714G>A
ENST00000538014.2:n.1733G>A
ENST00000585549.5:n.86G>A
ENST00000587095.1:n.84G>A
ENST00000588613.5:n.152G>A
ENST00000589075.5:n.125G>A
NR_045128.1:n.467G>A
NR_045129.1:n.467G>A