Canonical Allele Identifier: CA520136906
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751342A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589456A>C , CM000686.2:g.19589456A>C GRCh38
NC_000024.9:g.21751342A>C , CM000686.1:g.21751342A>C GRCh37
NC_000024.8:g.20210730A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.498-65A>C
ENST00000686905.1:n.1518A>C
ENST00000693214.1:n.1606A>C
ENST00000445715.6:n.400-65A>C
ENST00000407724.7:n.750-71A>C
ENST00000445715.5:n.400-65A>C
ENST00000447202.2:n.2370A>C
ENST00000447520.5:n.400-65A>C
ENST00000459719.6:n.1606A>C
ENST00000538014.2:n.1625A>C
ENST00000585549.5:n.43-65A>C
ENST00000587095.1:n.41-65A>C
ENST00000588613.5:n.109-65A>C
ENST00000589075.5:n.82-65A>C
NR_045128.1:n.424-65A>C
NR_045129.1:n.424-65A>C
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