Canonical Allele Identifier: CA2830536186

Gene: UTS2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.191268600A>G , CM000665.2:g.191268600A>G	GRCh38
NC_000003.11:g.190986389A>G , CM000665.1:g.190986389A>G	GRCh37
NC_000003.10:g.192469083A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340524.10:c.335-159T>C MANE Select	ENSP00000340526.5:n.335-159T>C
ENST00000340524.9:c.335-159T>C	ENSP00000340526.5:n.335-159T>C
ENST00000425357.1:c.*230-159T>C	ENSP00000404406.1:n.*230-159T>C
ENST00000427544.6:c.335-159T>C	ENSP00000398761.2:n.335-159T>C
ENST00000440476.5:c.*51-159T>C	ENSP00000398540.1:n.*51-159T>C
ENST00000446788.5:c.*115-159T>C	ENSP00000415628.1:n.*115-159T>C
NM_198152.3:c.335-159T>C	NP_937795.2:n.335-159T>C
XM_011512631.1:c.335-159T>C	XP_011510933.1:n.335-159T>C
XM_011512631.2:c.335-159T>C	XP_011510933.1:n.335-159T>C
NM_198152.4:c.335-159T>C	NP_937795.2:n.335-159T>C
NM_198152.5:c.335-159T>C MANE Select	NP_937795.2:n.335-159T>C