Canonical Allele Identifier: CA1979496252

Gene: SF3B2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66063320C= , CM000673.2:g.66063320C=	GRCh38
NC_000011.9:g.65830791C= , CM000673.1:g.65830791C=	GRCh37
NC_000011.8:g.65587367C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000322535.11:c.2086-80C= MANE Select	ENSP00000318861.6:n.2086-80C=
ENST00000322535.10:c.2086-80C=	ENSP00000318861.6:n.2086-80C=
ENST00000528302.5:c.2035-80C=	ENSP00000432655.1:n.2035-80C=
ENST00000530981.1:c.348-80C=
ENST00000610523.4:c.2014-80C=	ENSP00000482986.1:n.2014-80C=
NM_006842.2:c.2086-80C=	NP_006833.2:n.2086-80C=
XM_005273726.2:c.2083-80C=	XP_005273783.1:n.2083-80C=
XM_011544740.1:c.2083-80C=	XP_011543042.1:n.2083-80C=
XM_005273726.4:c.2083-80C=	XP_005273783.1:n.2083-80C=
XM_011544740.3:c.2083-80C=	XP_011543042.1:n.2083-80C=
XM_017017144.2:c.2080-80C=	XP_016872633.1:n.2080-80C=
NM_006842.3:c.2086-80C= MANE Select	NP_006833.2:n.2086-80C=