Canonical Allele Identifier: CA520136923
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751344A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589458A>C , CM000686.2:g.19589458A>C GRCh38
NC_000024.9:g.21751344A>C , CM000686.1:g.21751344A>C GRCh37
NC_000024.8:g.20210732A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000686158.1:n.498-63A>C
ENST00000686905.1:n.1520A>C
ENST00000693214.1:n.1608A>C
ENST00000445715.6:n.400-63A>C
ENST00000407724.7:n.750-69A>C
ENST00000445715.5:n.400-63A>C
ENST00000447202.2:n.2372A>C
ENST00000447520.5:n.400-63A>C
ENST00000459719.6:n.1608A>C
ENST00000538014.2:n.1627A>C
ENST00000585549.5:n.43-63A>C
ENST00000587095.1:n.41-63A>C
ENST00000588613.5:n.109-63A>C
ENST00000589075.5:n.82-63A>C
NR_045128.1:n.424-63A>C
NR_045129.1:n.424-63A>C