Canonical Allele Identifier: CA597098398

Gene:

Linked Data

• dbSNP Id: rs1334825656
• gnomAD v2: 11-2465772-G-GA
• gnomAD v3: 11-2444542-G-GA
• gnomAD v4: 11-2444542-G-GA
• MyVariant Identifiers: chr11:g.2465772_2465773insA (hg19) ; chr11:g.2444542_2444543insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2444543dup , CM000673.2:g.2444543dup	GRCh38
NC_000011.9:g.2465773dup , CM000673.1:g.2465773dup	GRCh37
NC_000011.8:g.2422349dup	NCBI36
NG_008935.1:g.4553dup , LRG_287:g.4553dup

Transcript Alleles

HGVS	Amino-acid Change
XR_930984.1:n.28dup