Canonical Allele Identifier: CA162478965
Gene: ABCB1 HGNC NCBI
RUNDC3B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2157926

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.87641184T>A , CM000669.2:g.87641184T>A GRCh38
NC_000007.13:g.87270500T>A , CM000669.1:g.87270500T>A GRCh37
NC_000007.12:g.87108436T>A NCBI36
NG_011513.1:g.77065A>T

Transcript Alleles

HGVS Amino-acid change
NM_000927.4:c.-330-40106A>T (ABCB1) VV NP_000918.2:p.=
NM_001134405.1:c.123-9638T>A (RUNDC3B) VV NP_001127877.1:p.=
NM_001134406.1:c.123-9638T>A (RUNDC3B) VV NP_001127878.1:p.=
NM_138290.2:c.123-9638T>A (RUNDC3B) VV NP_612147.1:p.=
XM_005250156.2:c.123-9638T>A (RUNDC3B) XP_005250213.1:p.=
XM_011515826.1:c.123-9638T>A (RUNDC3B) XP_011514128.1:p.=
XM_011515827.1:c.123-9638T>A (RUNDC3B) XP_011514129.1:p.=
XM_011515828.1:c.-221+5973T>A (RUNDC3B) XP_011514130.1:p.=
XM_011515829.1:c.-220-9638T>A (RUNDC3B) XP_011514131.1:p.=
NM_001348944.1:c.-183-40106A>T (ABCB1) VV NP_001335873.1:p.=
NM_001348945.1:c.-154-38044A>T (ABCB1) VV NP_001335874.1:p.=
XM_011515828.2:c.-221+5973T>A (RUNDC3B)
XM_011515829.2:c.-220-9638T>A (RUNDC3B)
XM_017011761.2:c.-349-9638T>A (RUNDC3B) XP_016867250.1:p.=
XM_017011762.1:c.-350+5973T>A (RUNDC3B) XP_016867251.1:p.=
XM_017011763.2:c.-105+12239T>A (RUNDC3B) XP_016867252.1:p.=
XM_017011765.2:c.-221+5973T>A (RUNDC3B) XP_016867254.1:p.=
XM_017011766.2:c.-349-9638T>A (RUNDC3B) XP_016867255.1:p.=
ENST00000265724.7:c.-330-40106A>T ENSP00000265724.3:p.=
ENST00000338056.7:c.123-9638T>A ENSP00000337732.3:p.=
ENST00000394654.3:c.123-9638T>A ENSP00000378149.3:p.=
ENST00000416177.1:c.-183-40106A>T ENSP00000399419.1:p.=
ENST00000466676.5:n.67-9638T>A
ENST00000476114.5:n.497-9638T>A
ENST00000476862.1:n.136-38044A>T
ENST00000489461.5:n.80-9638T>A
ENST00000493037.5:c.123-9638T>A ENSP00000420394.1:p.=
ENST00000497788.5:n.186-9638T>A
ENST00000543898.5:c.-330-40106A>T ENSP00000444095.1:p.=