Canonical Allele Identifier: CA756174344

Gene:

Linked Data

• dbSNP Id: rs1286403082
• MyVariant Identifiers: chr2:g.123126461_123126462insT (hg19) ; chr2:g.122368885_122368886insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122368886dup , CM000664.2:g.122368886dup	GRCh38
NC_000002.11:g.123126462dup , CM000664.1:g.123126462dup	GRCh37
NC_000002.10:g.122842932dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-24077dup
XR_001739684.1:n.556-24077dup