Canonical Allele Identifier: CA520136053
Gene: TXLNGY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21751246A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19589360A>C , CM000686.2:g.19589360A>C GRCh38
NC_000024.9:g.21751246A>C , CM000686.1:g.21751246A>C GRCh37
NC_000024.8:g.20210634A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000686158.1:n.498-161A>C
ENST00000686905.1:n.1422A>C
ENST00000693214.1:n.1510A>C
ENST00000445715.6:n.400-161A>C
ENST00000407724.7:n.750-167A>C
ENST00000445715.5:n.400-161A>C
ENST00000447202.2:n.2274A>C
ENST00000447520.5:n.400-161A>C
ENST00000459719.6:n.1510A>C
ENST00000538014.2:n.1529A>C
ENST00000585549.5:n.43-161A>C
ENST00000587095.1:n.41-161A>C
ENST00000588613.5:n.109-161A>C
ENST00000589075.5:n.82-161A>C
NR_045128.1:n.424-161A>C
NR_045129.1:n.424-161A>C
Search 100 bp 5'
Search 100 bp 3'