Canonical Allele Identifier: CA860367879

Gene:

Linked Data

• dbSNP Id: rs1230639318
• MyVariant Identifiers: chr9:g.132339100_132339101insT (hg19) ; chr9:g.129576821_129576822insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576821_129576822insT , CM000671.2:g.129576821_129576822insT	GRCh38
NC_000009.11:g.132339100_132339101insT , CM000671.1:g.132339100_132339101insT	GRCh37
NC_000009.10:g.131378921_131378922insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1223_182+1224insT