Canonical Allele Identifier: CA520139027
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751567A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589681A>C , CM000686.2:g.19589681A>C GRCh38
NC_000024.9:g.21751567A>C , CM000686.1:g.21751567A>C GRCh37
NC_000024.8:g.20210955A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.589+69A>C
ENST00000686905.1:n.1743A>C
ENST00000693214.1:n.1831A>C
ENST00000445715.6:n.491+69A>C
ENST00000407724.7:n.835+69A>C
ENST00000445715.5:n.491+69A>C
ENST00000447202.2:n.2595A>C
ENST00000447520.5:n.491+69A>C
ENST00000459719.6:n.1762+69A>C
ENST00000538014.2:n.1850A>C
ENST00000585549.5:n.134+69A>C
ENST00000587095.1:n.132+69A>C
ENST00000588613.5:n.200+69A>C
ENST00000589075.5:n.173+69A>C
NR_045128.1:n.515+69A>C
NR_045129.1:n.515+69A>C
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