Canonical Allele Identifier: CA675189407

Gene:

Linked Data

• dbSNP Id: rs1212543929
• gnomAD v4: 11-27484081-C-CA
• MyVariant Identifiers: chr11:g.27505628_27505629insA (hg19) ; chr11:g.27484081_27484082insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484082dup , CM000673.2:g.27484082dup	GRCh38
NC_000011.9:g.27505629dup , CM000673.1:g.27505629dup	GRCh37
NC_000011.8:g.27462205dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.233dup