Canonical Allele Identifier: CA520137774
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751433G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589547G>C , CM000686.2:g.19589547G>C GRCh38
NC_000024.9:g.21751433G>C , CM000686.1:g.21751433G>C GRCh37
NC_000024.8:g.20210821G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.524G>C
ENST00000686905.1:n.1609G>C
ENST00000693214.1:n.1697G>C
ENST00000445715.6:n.426G>C
ENST00000407724.7:n.770G>C
ENST00000445715.5:n.426G>C
ENST00000447202.2:n.2461G>C
ENST00000447520.5:n.426G>C
ENST00000459719.6:n.1697G>C
ENST00000538014.2:n.1716G>C
ENST00000585549.5:n.69G>C
ENST00000587095.1:n.67G>C
ENST00000588613.5:n.135G>C
ENST00000589075.5:n.108G>C
NR_045128.1:n.450G>C
NR_045129.1:n.450G>C
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