Canonical Allele Identifier: CA520136637
Gene: TXLNGY HGNC NCBI

Linked Data

gnomAD v3: Y-19589427-C-G
gnomAD v4: Y-19589427-C-G
MyVariant Identifiers: chrY:g.21751313C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589427C>G , CM000686.2:g.19589427C>G GRCh38
NC_000024.9:g.21751313C>G , CM000686.1:g.21751313C>G GRCh37
NC_000024.8:g.20210701C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.498-94C>G
ENST00000686905.1:n.1489C>G
ENST00000693214.1:n.1577C>G
ENST00000445715.6:n.400-94C>G
ENST00000407724.7:n.750-100C>G
ENST00000445715.5:n.400-94C>G
ENST00000447202.2:n.2341C>G
ENST00000447520.5:n.400-94C>G
ENST00000459719.6:n.1577C>G
ENST00000538014.2:n.1596C>G
ENST00000585549.5:n.43-94C>G
ENST00000587095.1:n.41-94C>G
ENST00000588613.5:n.109-94C>G
ENST00000589075.5:n.82-94C>G
NR_045128.1:n.424-94C>G
NR_045129.1:n.424-94C>G
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