Allele Registry

Canonical Allele Identifier: CA337549529

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrY:g.6794671C>T

GRCh37 chrY:g.6662712C>T

Linked Data - Sequence & Population

gnomAD v3:

Y:6794671 C / T

gnomAD v4:

chrY-6794671-C-T

Joint Max Group AF 0.18098528 (NFE)

Genomes Max Group AF 0.18098528 (NFE)

Linked Data - NCBI & NCI

dbSNP:

112137450

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.6794671C>T , CM000686.2:g.6794671C>T	GRCh38
NC_000024.9:g.6662712C>T , CM000686.1:g.6662712C>T	GRCh37
NC_000024.8:g.6722712C>T	NCBI36

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