Canonical Allele Identifier: CA10654692

Gene:

Linked Data

• ClinVar Variation Id: 369511
• ClinVar RCV Id: RCV000307781
• dbSNP Id: rs112734053
• gnomAD v2: 6-108188948-G-GA
• gnomAD v3: 6-107867744-G-GA
• gnomAD v4: 6-107867744-G-GA
• MyVariant Identifiers: chr6:g.108188949dupA (hg19) ; chr6:g.108188948_108188949insA (hg19) ; chr6:g.107867745dupA (hg38) ; chr6:g.107867744_107867745insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107867755dup , CM000668.2:g.107867755dup	GRCh38
NC_000006.11:g.108188959dup , CM000668.1:g.108188959dup	GRCh37
NC_000006.10:g.108295652dup	NCBI36
NG_008270.1:g.95534dup