ClinGen Allele Registry
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Canonical Allele Identifier:
CA337486997
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.20351840A>C
GRCh37
chrY:g.22513726A>C
Linked Data - NCBI & NCI
dbSNP:
3906451
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.20351840A>C , CM000686.2:g.20351840A>C
GRCh38
NC_000024.9:g.22513726A>C , CM000686.1:g.22513726A>C
GRCh37
NC_000024.8:g.20923114A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'