Canonical Allele Identifier: CA520138369
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751495T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589609T>G , CM000686.2:g.19589609T>G GRCh38
NC_000024.9:g.21751495T>G , CM000686.1:g.21751495T>G GRCh37
NC_000024.8:g.20210883T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.586T>G
ENST00000686905.1:n.1671T>G
ENST00000693214.1:n.1759T>G
ENST00000445715.6:n.488T>G
ENST00000407724.7:n.832T>G
ENST00000445715.5:n.488T>G
ENST00000447202.2:n.2523T>G
ENST00000447520.5:n.488T>G
ENST00000459719.6:n.1759T>G
ENST00000538014.2:n.1778T>G
ENST00000585549.5:n.131T>G
ENST00000587095.1:n.129T>G
ENST00000588613.5:n.197T>G
ENST00000589075.5:n.170T>G
NR_045128.1:n.512T>G
NR_045129.1:n.512T>G
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