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Canonical Allele Identifier:
CA337490538
Gene: TTTY10
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrY:g.20509720T>C
GRCh37
chrY:g.22671606T>C
Linked Data - Sequence & Population
gnomAD v3:
Y:20509720 T / C
gnomAD v4:
chrY-20509720-T-C
Joint Max Group AF
0.18668459 (MID)
Genomes Max Group AF
0.0742162 (AMR)
Linked Data - NCBI & NCI
dbSNP:
369537498
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.20509720T>C , CM000686.2:g.20509720T>C
GRCh38
NC_000024.9:g.22671606T>C , CM000686.1:g.22671606T>C
GRCh37
NC_000024.8:g.21080994T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_001542.1:n.959-2264A>G
Search 100 bp 5'
Search 100 bp 3'