ClinGen Allele Registry
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Canonical Allele Identifier:
CA337744435
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.14180986G>A
GRCh37
chrY:g.16292866G>A
Linked Data - Sequence & Population
gnomAD v3:
Y:14180986 G / A
gnomAD v4:
chrY-14180986-G-A
Joint Max Group AF
0.00125879 (AFR)
Genomes Max Group AF
0.00125879 (AFR)
Linked Data - NCBI & NCI
dbSNP:
187287389
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.14180986G>A , CM000686.2:g.14180986G>A
GRCh38
NC_000024.9:g.16292866G>A , CM000686.1:g.16292866G>A
GRCh37
NC_000024.8:g.14802260G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'