Canonical Allele Identifier: CA520137547
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751409A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589523A>G , CM000686.2:g.19589523A>G GRCh38
NC_000024.9:g.21751409A>G , CM000686.1:g.21751409A>G GRCh37
NC_000024.8:g.20210797A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.500A>G
ENST00000686905.1:n.1585A>G
ENST00000693214.1:n.1673A>G
ENST00000445715.6:n.402A>G
ENST00000407724.7:n.750-4A>G
ENST00000445715.5:n.402A>G
ENST00000447202.2:n.2437A>G
ENST00000447520.5:n.402A>G
ENST00000459719.6:n.1673A>G
ENST00000538014.2:n.1692A>G
ENST00000585549.5:n.45A>G
ENST00000587095.1:n.43A>G
ENST00000588613.5:n.111A>G
ENST00000589075.5:n.84A>G
NR_045128.1:n.426A>G
NR_045129.1:n.426A>G
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