Allele Registry

Canonical Allele Identifier: CA337742342

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrY:g.14091100C>G

GRCh37 chrY:g.16202980C>G

Linked Data - Sequence & Population

gnomAD v3:

Y:14091100 C / G

gnomAD v4:

chrY-14091100-C-G

Joint Max Group AF 0.80264859 (EAS)

Genomes Max Group AF 0.80264859 (EAS)

Linked Data - NCBI & NCI

dbSNP:

16980363

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.14091100C>G , CM000686.2:g.14091100C>G	GRCh38
NC_000024.9:g.16202980C>G , CM000686.1:g.16202980C>G	GRCh37
NC_000024.8:g.14712374C>G	NCBI36

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