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Canonical Allele Identifier:
CA337489820
Gene: TTTY10
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrY:g.20472878A>C
GRCh37
chrY:g.22634764A>C
Linked Data - Sequence & Population
gnomAD v3:
Y:20472878 A / C
gnomAD v4:
chrY-20472878-A-C
Joint Max Group AF
0.55302303 (AFR)
Genomes Max Group AF
0.55302303 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9785892
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.20472878A>C , CM000686.2:g.20472878A>C
GRCh38
NC_000024.9:g.22634764A>C , CM000686.1:g.22634764A>C
GRCh37
NC_000024.8:g.21044152A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_001542.1:n.1064-2897T>G
Search 100 bp 5'
Search 100 bp 3'