Canonical Allele Identifier: CA520137871
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751441C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589555C>G , CM000686.2:g.19589555C>G GRCh38
NC_000024.9:g.21751441C>G , CM000686.1:g.21751441C>G GRCh37
NC_000024.8:g.20210829C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.532C>G
ENST00000686905.1:n.1617C>G
ENST00000693214.1:n.1705C>G
ENST00000445715.6:n.434C>G
ENST00000407724.7:n.778C>G
ENST00000445715.5:n.434C>G
ENST00000447202.2:n.2469C>G
ENST00000447520.5:n.434C>G
ENST00000459719.6:n.1705C>G
ENST00000538014.2:n.1724C>G
ENST00000585549.5:n.77C>G
ENST00000587095.1:n.75C>G
ENST00000588613.5:n.143C>G
ENST00000589075.5:n.116C>G
NR_045128.1:n.458C>G
NR_045129.1:n.458C>G
Search 100 bp 5'
Search 100 bp 3'