Allele Registry

Canonical Allele Identifier: CA14703614

Gene:

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr19:g.44905579T>G

GRCh37 chr19:g.45408836T>G

Linked Data - Sequence & Population

gnomAD v2:

19:45408836 T / G

gnomAD v3:

19:44905579 T / G

gnomAD v4:

chr19-44905579-T-G

Joint Max Group AF 0.73978203 (AFR)

Genomes Max Group AF 0.73978203 (AFR)

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000845578

ClinVar Variation:

619951

dbSNP:

405509

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905579T>G , CM000681.2:g.44905579T>G	GRCh38
NC_000019.9:g.45408836T>G , CM000681.1:g.45408836T>G	GRCh37
NC_000019.8:g.50100676T>G	NCBI36
NG_007084.2:g.4798T>G
NG_042854.1:g.19360T>G

Search 100 bp 5'

Search 100 bp 3'