Canonical Allele Identifier: CA2194510027
Gene: RLBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211692C= , CM000677.2:g.89211692C= GRCh38
NC_000015.9:g.89754923C= , CM000677.1:g.89754923C= GRCh37
NC_000015.8:g.87555927C= NCBI36
NG_008116.1:g.15000G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268125.10:c.684+51G= MANE Select ENSP00000268125.5:n.684+51G=
ENST00000268125.9:c.684+51G= ENSP00000268125.5:n.684+51G=
ENST00000563254.1:c.101+51G=
ENST00000567787.1:c.*262+51G= ENSP00000457251.1:n.*262+51G=
NM_000326.4:c.684+51G= NP_000317.1:n.684+51G=
XM_011521870.1:c.684+51G= XP_011520172.1:n.684+51G=
XM_011521871.1:c.609+51G= XP_011520173.1:n.609+51G=
XM_011521872.1:c.609+51G= XP_011520174.1:n.609+51G=
XM_011521870.2:c.684+51G= XP_011520172.1:n.684+51G=
XM_017022460.1:c.711+51G= XP_016877949.1:n.711+51G=
NM_000326.5:c.684+51G= MANE Select NP_000317.1:n.684+51G=