Canonical Allele Identifier: CA337627617
Gene: TTTY11 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.8812620C>T
GRCh37 chrY:g.8680661C>T
gnomAD v3:
Y:8812620 C / T
gnomAD v4:
chrY-8812620-C-T
Joint Max Group AF 0.70140507 (AFR)
Genomes Max Group AF 0.70140507 (AFR)
dbSNP:
9786707
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8812620C>T , CM000686.2:g.8812620C>T GRCh38
NC_000024.9:g.8680661C>T , CM000686.1:g.8680661C>T GRCh37
NC_000024.8:g.8740661C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000253470.4:n.37+4726G>A
NR_001548.2:n.37+4726G>A
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