Allele Registry

Canonical Allele Identifier: CA336265826

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chrX:g.136644791A>G

GRCh37 chrX:g.135726950A>G

Linked Data - Sequence & Population

gnomAD v2:

X:135726950 A / G

gnomAD v3:

X:136644791 A / G

gnomAD v4:

chrX-136644791-A-G

Joint Max Group AF 0.46047647 (AFR)

Genomes Max Group AF 0.46047647 (AFR)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV001811567

ClinVar Variation:

810925

dbSNP:

3092952

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136644791A>G , CM000685.2:g.136644791A>G	GRCh38
NC_000023.10:g.135726950A>G , CM000685.1:g.135726950A>G	GRCh37
NC_000023.9:g.135554616A>G	NCBI36
NG_007280.1:g.1615A>G , LRG_141:g.1615A>G

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