Allele Registry

Canonical Allele Identifier: CA14645745

Gene:

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr19:g.48954681A>G

GRCh37 chr19:g.49457938A>G

Linked Data - Sequence & Population

gnomAD v2:

19:49457938 A / G

gnomAD v3:

19:48954681 A / G

gnomAD v4:

chr19-48954681-A-G

Joint Max Group AF 0.95454193 (EAS)

Genomes Max Group AF 0.92956086 (EAS)

Exomes Max Group AF 0.95644995 (EAS)

Linked Data - NCBI & NCI

dbSNP:

4645878

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48954681A>G , CM000681.2:g.48954681A>G	GRCh38
NC_000019.9:g.49457938A>G , CM000681.1:g.49457938A>G	GRCh37
NC_000019.8:g.54149750A>G	NCBI36
NG_012191.1:g.4822A>G

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