Canonical Allele Identifier: CA520137064
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751356G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589470G>C , CM000686.2:g.19589470G>C GRCh38
NC_000024.9:g.21751356G>C , CM000686.1:g.21751356G>C GRCh37
NC_000024.8:g.20210744G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.498-51G>C
ENST00000686905.1:n.1532G>C
ENST00000693214.1:n.1620G>C
ENST00000445715.6:n.400-51G>C
ENST00000407724.7:n.750-57G>C
ENST00000445715.5:n.400-51G>C
ENST00000447202.2:n.2384G>C
ENST00000447520.5:n.400-51G>C
ENST00000459719.6:n.1620G>C
ENST00000538014.2:n.1639G>C
ENST00000585549.5:n.43-51G>C
ENST00000587095.1:n.41-51G>C
ENST00000588613.5:n.109-51G>C
ENST00000589075.5:n.82-51G>C
NR_045128.1:n.424-51G>C
NR_045129.1:n.424-51G>C