Canonical Allele Identifier: CA660863685

Gene:

Linked Data

• dbSNP Id: rs1198509947
• MyVariant Identifiers: chr10:g.124217790_124217791insC (hg19) ; chr10:g.122458274_122458275insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122458274_122458275insC , CM000672.2:g.122458274_122458275insC	GRCh38
NC_000010.10:g.124217790_124217791insC , CM000672.1:g.124217790_124217791insC	GRCh37
NC_000010.9:g.124207780_124207781insC	NCBI36
NG_011554.1:g.1750_1751insC
NG_011725.1:g.8612_8613insC

Transcript Alleles

HGVS	Amino-acid Change
XR_946382.1:n.1827+220_1827+221insG
XR_946383.1:n.1827+220_1827+221insG
XR_946384.1:n.1576+220_1576+221insG
XR_946385.1:n.1827+220_1827+221insG
XR_946382.2:n.1855+220_1855+221insG
XR_946383.2:n.1855+220_1855+221insG
XR_946384.2:n.1580+220_1580+221insG
XR_946385.2:n.1855+220_1855+221insG