Canonical Allele Identifier: CA10574576
Gene: TXLNGY HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.19589554A>C
GRCh37 chrY:g.21751440A>C
Revel Score:
ENST00000447520 0.174
gnomAD v2:
Y:21751440 A / C
gnomAD v3:
Y:19589554 A / C
gnomAD v4:
chrY-19589554-A-C
Joint Max Group AF 0.00975315 (EAS)
Genomes Max Group AF 0.01754756 (EAS)
Exomes Max Group AF 0.00775221 (EAS)
dbSNP:
72622300
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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
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