Canonical Allele Identifier: CA77246677

Gene:

Linked Data

• dbSNP Id: rs71699003
• MyVariant Identifiers: chr3:g.72315980_72315981insCA (hg19) ; chr3:g.72266829_72266830insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.72266829_72266830insCA , CM000665.2:g.72266829_72266830insCA	GRCh38
NC_000003.11:g.72315980_72315981insCA , CM000665.1:g.72315980_72315981insCA	GRCh37
NC_000003.10:g.72398670_72398671insCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940958.1:n.835+8278_835+8279insTG