Canonical Allele Identifier: CA520136956
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751345T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589459T>C , CM000686.2:g.19589459T>C GRCh38
NC_000024.9:g.21751345T>C , CM000686.1:g.21751345T>C GRCh37
NC_000024.8:g.20210733T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.498-62T>C
ENST00000686905.1:n.1521T>C
ENST00000693214.1:n.1609T>C
ENST00000445715.6:n.400-62T>C
ENST00000407724.7:n.750-68T>C
ENST00000445715.5:n.400-62T>C
ENST00000447202.2:n.2373T>C
ENST00000447520.5:n.400-62T>C
ENST00000459719.6:n.1609T>C
ENST00000538014.2:n.1628T>C
ENST00000585549.5:n.43-62T>C
ENST00000587095.1:n.41-62T>C
ENST00000588613.5:n.109-62T>C
ENST00000589075.5:n.82-62T>C
NR_045128.1:n.424-62T>C
NR_045129.1:n.424-62T>C