Canonical Allele Identifier: CA17270698

Gene: UTS2

Linked Data

• dbSNP Id: rs36079839
• MyVariant Identifiers: chr1:g.7961252_7961253insC (hg19) ; chr1:g.7901192_7901193insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7901192_7901193insC , CM000663.2:g.7901192_7901193insC	GRCh38
NC_000001.10:g.7961252_7961253insC , CM000663.1:g.7961252_7961253insC	GRCh37
NC_000001.9:g.7883839_7883840insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011540537.1:c.-75+11988_-75+11989insG	XP_011538839.1:n.-75+11988_-75+11989insG
XM_011540537.2:c.-75+11988_-75+11989insG	XP_011538839.1:n.-75+11988_-75+11989insG
XM_017000116.1:c.-75+11988_-75+11989insG	XP_016855605.1:n.-75+11988_-75+11989insG
XM_017000119.1:c.-75+11988_-75+11989insG	XP_016855608.1:n.-75+11988_-75+11989insG