Canonical Allele Identifier: CA520136980
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751348A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589462A>C , CM000686.2:g.19589462A>C GRCh38
NC_000024.9:g.21751348A>C , CM000686.1:g.21751348A>C GRCh37
NC_000024.8:g.20210736A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.498-59A>C
ENST00000686905.1:n.1524A>C
ENST00000693214.1:n.1612A>C
ENST00000445715.6:n.400-59A>C
ENST00000407724.7:n.750-65A>C
ENST00000445715.5:n.400-59A>C
ENST00000447202.2:n.2376A>C
ENST00000447520.5:n.400-59A>C
ENST00000459719.6:n.1612A>C
ENST00000538014.2:n.1631A>C
ENST00000585549.5:n.43-59A>C
ENST00000587095.1:n.41-59A>C
ENST00000588613.5:n.109-59A>C
ENST00000589075.5:n.82-59A>C
NR_045128.1:n.424-59A>C
NR_045129.1:n.424-59A>C
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