Canonical Allele Identifier: CA569081

Gene: UTS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7853370G>A , CM000663.2:g.7853370G>A	GRCh38
NC_000001.10:g.7913430G>A , CM000663.1:g.7913430G>A	GRCh37
NC_000001.9:g.7836017G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021995.2:c.62C>T	NP_068835.1:p.Thr21Met
ENST00000054668.5:c.62C>T	ENSP00000054668.5:p.Thr21Met
ENST00000377516.6:c.-179C>T	ENSP00000366738.2:n.-179C>T
XM_011540537.1:c.62C>T	XP_011538839.1:p.Thr21Met
XM_011540537.2:c.62C>T	XP_011538839.1:p.Thr21Met
XM_011540538.1:c.-181C>T	XP_011538840.1:n.-181C>T
XM_017000116.1:c.62C>T	XP_016855605.1:p.Thr21Met
XM_017000117.1:c.-181C>T	XP_016855606.1:n.-181C>T
XM_017000118.1:c.-51C>T	XP_016855607.1:n.-51C>T
XM_017000119.1:c.62C>T	XP_016855608.1:p.Thr21Met