Canonical Allele Identifier: CA1723681903

Gene: RUNDC3B ABCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87641127C= , CM000669.2:g.87641127C=	GRCh38
NC_000007.13:g.87270443C= , CM000669.1:g.87270443C=	GRCh37
NC_000007.12:g.87108379C=	NCBI36
NG_011513.1:g.77122G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394654.4:c.123-9695C= (RUNDC3B) MANE Select	ENSP00000378149.3:n.123-9695C=
ENST00000265724.8:c.-330-40049G= (ABCB1)	ENSP00000265724.3:n.-330-40049G=
ENST00000265724.7:c.-330-40049G= (ABCB1)	ENSP00000265724.3:n.-330-40049G=
ENST00000338056.7:c.123-9695C= (RUNDC3B)	ENSP00000337732.3:n.123-9695C=
ENST00000394654.3:c.123-9695C= (RUNDC3B)	ENSP00000378149.3:n.123-9695C=
ENST00000416177.1:c.-183-40049G= (ABCB1)	ENSP00000399419.1:n.-183-40049G=
ENST00000466676.5:n.67-9695C= (RUNDC3B)
ENST00000476114.5:n.497-9695C= (RUNDC3B)
ENST00000476862.1:n.136-37987G= (ABCB1)
ENST00000489461.5:n.80-9695C= (RUNDC3B)
ENST00000493037.5:c.123-9695C= (RUNDC3B)	ENSP00000420394.1:n.123-9695C=
ENST00000497788.5:n.186-9695C= (RUNDC3B)
ENST00000543898.5:c.-330-40049G= (ABCB1)	ENSP00000444095.1:n.-330-40049G=
NM_000927.4:c.-330-40049G= (ABCB1)	NP_000918.2:n.-330-40049G=
NM_001134405.1:c.123-9695C= (RUNDC3B)	NP_001127877.1:n.123-9695C=
NM_001134406.1:c.123-9695C= (RUNDC3B)	NP_001127878.1:n.123-9695C=
NM_138290.2:c.123-9695C= (RUNDC3B)	NP_612147.1:n.123-9695C=
XM_005250156.2:c.123-9695C= (RUNDC3B)	XP_005250213.1:n.123-9695C=
XM_011515826.1:c.123-9695C= (RUNDC3B)	XP_011514128.1:n.123-9695C=
XM_011515827.1:c.123-9695C= (RUNDC3B)	XP_011514129.1:n.123-9695C=
XM_011515828.1:c.-221+5916C= (RUNDC3B)	XP_011514130.1:n.-221+5916C=
XM_011515829.1:c.-220-9695C= (RUNDC3B)	XP_011514131.1:n.-220-9695C=
NM_001348944.1:c.-183-40049G= (ABCB1)	NP_001335873.1:n.-183-40049G=
NM_001348945.1:c.-154-37987G= (ABCB1)	NP_001335874.1:n.-154-37987G=
XM_011515828.2:c.-221+5916C= (RUNDC3B)	XP_011514130.1:n.-221+5916C=
XM_011515829.2:c.-220-9695C= (RUNDC3B)	XP_011514131.1:n.-220-9695C=
XM_017011761.2:c.-349-9695C= (RUNDC3B)	XP_016867250.1:n.-349-9695C=
XM_017011762.1:c.-350+5916C= (RUNDC3B)	XP_016867251.1:n.-350+5916C=
XM_017011763.2:c.-105+12182C= (RUNDC3B)	XP_016867252.1:n.-105+12182C=
XM_017011765.2:c.-221+5916C= (RUNDC3B)	XP_016867254.1:n.-221+5916C=
XM_017011766.2:c.-349-9695C= (RUNDC3B)	XP_016867255.1:n.-349-9695C=
NM_001134405.2:c.123-9695C= (RUNDC3B) MANE Select	NP_001127877.1:n.123-9695C=
NM_001134406.2:c.123-9695C= (RUNDC3B)	NP_001127878.1:n.123-9695C=
NM_138290.3:c.123-9695C= (RUNDC3B)	NP_612147.1:n.123-9695C=
NM_000927.5:c.-330-40049G= (ABCB1)	NP_000918.2:n.-330-40049G=
NM_001348944.2:c.-183-40049G= (ABCB1)	NP_001335873.1:n.-183-40049G=
NM_001348945.2:c.-154-37987G= (ABCB1)	NP_001335874.1:n.-154-37987G=
NM_001394224.1:c.123-9695C= (RUNDC3B)	NP_001381153.1:n.123-9695C=
NM_001394225.1:c.123-9695C= (RUNDC3B)	NP_001381154.1:n.123-9695C=
NM_001394226.1:c.123-9695C= (RUNDC3B)	NP_001381155.1:n.123-9695C=
NM_001394227.1:c.123-9695C= (RUNDC3B)	NP_001381156.1:n.123-9695C=
NM_001394228.1:c.-220-9695C= (RUNDC3B)	NP_001381157.1:n.-220-9695C=