Canonical Allele Identifier: CA759294477

Gene:

Linked Data

• dbSNP Id: rs1311956432
• gnomAD v3: 2-155870637-G-GT
• gnomAD v4: 2-155870637-G-GT
• MyVariant Identifiers: chr2:g.156727149_156727150insT (hg19) ; chr2:g.155870637_155870638insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.155870638dup , CM000664.2:g.155870638dup	GRCh38
NC_000002.11:g.156727150dup , CM000664.1:g.156727150dup	GRCh37
NC_000002.10:g.156435396dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923501.1:n.320-3451dup
XR_001739749.1:n.331-29654dup
XR_001739750.1:n.331-29654dup
XR_001739751.1:n.331-29654dup
XR_923501.2:n.331-3451dup