Canonical Allele Identifier: CA520137990
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751452C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589566C>A , CM000686.2:g.19589566C>A GRCh38
NC_000024.9:g.21751452C>A , CM000686.1:g.21751452C>A GRCh37
NC_000024.8:g.20210840C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.543C>A
ENST00000686905.1:n.1628C>A
ENST00000693214.1:n.1716C>A
ENST00000445715.6:n.445C>A
ENST00000407724.7:n.789C>A
ENST00000445715.5:n.445C>A
ENST00000447202.2:n.2480C>A
ENST00000447520.5:n.445C>A
ENST00000459719.6:n.1716C>A
ENST00000538014.2:n.1735C>A
ENST00000585549.5:n.88C>A
ENST00000587095.1:n.86C>A
ENST00000588613.5:n.154C>A
ENST00000589075.5:n.127C>A
NR_045128.1:n.469C>A
NR_045129.1:n.469C>A
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