Canonical Allele Identifier: CA763204562

Gene:

Linked Data

• dbSNP Id: rs1337711791
• MyVariant Identifiers: chr2:g.200897896_200897897insT (hg19) ; chr2:g.200033173_200033174insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033177dup , CM000664.2:g.200033177dup	GRCh38
NC_000002.11:g.200897900dup , CM000664.1:g.200897900dup	GRCh37
NC_000002.10:g.200606145dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22278dup