ClinGen Allele Registry
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Canonical Allele Identifier:
CA337135708
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.15533455G>A
GRCh37
chrY:g.17645335G>A
Linked Data - NCBI & NCI
dbSNP:
191193873
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.15533455G>A , CM000686.2:g.15533455G>A
GRCh38
NC_000024.9:g.17645335G>A , CM000686.1:g.17645335G>A
GRCh37
NC_000024.8:g.16154729G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'