Canonical Allele Identifier: CA755748291

Gene:

Linked Data

• dbSNP Id: rs1448082641
• MyVariant Identifiers: chr2:g.118837202_118837203insA (hg19) ; chr2:g.118079626_118079627insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118079631dup , CM000664.2:g.118079631dup	GRCh38
NC_000002.11:g.118837207dup , CM000664.1:g.118837207dup	GRCh37
NC_000002.10:g.118553677dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011512305.1:c.697-2095dup	XP_011510607.1:n.697-2095dup
XR_001739662.2:n.138+8624dup