Canonical Allele Identifier: CA337627606
Gene: TTTY11 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.8811802T>G
GRCh37 chrY:g.8679843T>G
gnomAD v3:
Y:8811802 T / G
gnomAD v4:
chrY-8811802-T-G
Joint Max Group AF 0.76613882 (AFR)
Genomes Max Group AF 0.76613882 (AFR)
dbSNP:
3853054
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8811802T>G , CM000686.2:g.8811802T>G GRCh38
NC_000024.9:g.8679843T>G , CM000686.1:g.8679843T>G GRCh37
NC_000024.8:g.8739843T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253470.4:n.37+5544A>C
NR_001548.2:n.37+5544A>C
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