Canonical Allele Identifier: CA98367597

Gene:

Linked Data

• dbSNP Id: rs869276235
• MyVariant Identifiers: chr4:g.63424166_63424167insA (hg19) ; chr4:g.62558448_62558449insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.62558448_62558449insA , CM000666.2:g.62558448_62558449insA	GRCh38
NC_000004.11:g.63424166_63424167insA , CM000666.1:g.63424166_63424167insA	GRCh37
NC_000004.10:g.63106761_63106762insA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_938814.1:n.161-5396_161-5395insA