ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA337767752
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.15282231C>G
GRCh37
chrY:g.17394111C>G
Linked Data - Sequence & Population
gnomAD v3:
Y:15282231 C / G
gnomAD v4:
chrY-15282231-C-G
Joint Max Group AF
0.6052969 (AFR)
Genomes Max Group AF
0.6052969 (AFR)
Linked Data - NCBI & NCI
dbSNP:
9785940
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.15282231C>G , CM000686.2:g.15282231C>G
GRCh38
NC_000024.9:g.17394111C>G , CM000686.1:g.17394111C>G
GRCh37
NC_000024.8:g.15903505C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_001756089.1:n.310-35053G>C
Search 100 bp 5'
Search 100 bp 3'