ClinGen Allele Registry
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Canonical Allele Identifier:
CA337742817
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.14110761G>C
GRCh37
chrY:g.16222641G>C
Linked Data - Sequence & Population
gnomAD v3:
Y:14110761 G / C
gnomAD v4:
chrY-14110761-G-C
Linked Data - NCBI & NCI
dbSNP:
779917018
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.14110761G>C , CM000686.2:g.14110761G>C
GRCh38
NC_000024.9:g.16222641G>C , CM000686.1:g.16222641G>C
GRCh37
NC_000024.8:g.14732035G>C
NCBI36
Search 100 bp 5'
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