Canonical Allele Identifier: CA10574576

Gene: TXLNGY

Linked Data

• dbSNP Id: rs72622300
• ExAC: Y:21751440 A / C
• gnomAD v2: Y-21751440-A-C
• gnomAD v3: Y-19589554-A-C
• gnomAD v4: Y-19589554-A-C
• MyVariant Identifiers: chrY:g.21751440A>C (hg19) ; chrY:g.19589554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19589554A>C , CM000686.2:g.19589554A>C	GRCh38
NC_000024.9:g.21751440A>C , CM000686.1:g.21751440A>C	GRCh37
NC_000024.8:g.20210828A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000686158.1:n.531A>C
ENST00000686905.1:n.1616A>C
ENST00000693214.1:n.1704A>C
ENST00000445715.6:n.433A>C
ENST00000407724.7:n.777A>C
ENST00000445715.5:n.433A>C
ENST00000447202.2:n.2468A>C
ENST00000447520.5:n.433A>C
ENST00000459719.6:n.1704A>C
ENST00000538014.2:n.1723A>C
ENST00000585549.5:n.76A>C
ENST00000587095.1:n.74A>C
ENST00000588613.5:n.142A>C
ENST00000589075.5:n.115A>C
NR_045128.1:n.457A>C
NR_045129.1:n.457A>C