Canonical Allele Identifier: CA2194510051
Gene: RLBP1 HGNC NCBI

Linked Data

dbSNP Id: rs2051539257

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211700C>G , CM000677.2:g.89211700C>G GRCh38
NC_000015.9:g.89754931C>G , CM000677.1:g.89754931C>G GRCh37
NC_000015.8:g.87555935C>G NCBI36
NG_008116.1:g.14992G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000268125.10:c.684+43G>C MANE Select ENSP00000268125.5:n.684+43G>C
ENST00000268125.9:c.684+43G>C ENSP00000268125.5:n.684+43G>C
ENST00000563254.1:c.101+43G>C
ENST00000567787.1:c.*262+43G>C ENSP00000457251.1:n.*262+43G>C
NM_000326.4:c.684+43G>C NP_000317.1:n.684+43G>C
XM_011521870.1:c.684+43G>C XP_011520172.1:n.684+43G>C
XM_011521871.1:c.609+43G>C XP_011520173.1:n.609+43G>C
XM_011521872.1:c.609+43G>C XP_011520174.1:n.609+43G>C
XM_011521870.2:c.684+43G>C XP_011520172.1:n.684+43G>C
XM_017022460.1:c.711+43G>C XP_016877949.1:n.711+43G>C
NM_000326.5:c.684+43G>C MANE Select NP_000317.1:n.684+43G>C