Canonical Allele Identifier: CA492076167
Gene: RLBP1 HGNC NCBI

Linked Data

dbSNP Id: rs2051540700
MyVariant Identifiers: chr15:g.89755052C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211821C>T , CM000677.2:g.89211821C>T GRCh38
NC_000015.9:g.89755052C>T , CM000677.1:g.89755052C>T GRCh37
NC_000015.8:g.87556056C>T NCBI36
NG_008116.1:g.14871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000268125.10:c.606G>A MANE Select ENSP00000268125.5:p.Glu202=
ENST00000268125.9:c.606G>A ENSP00000268125.5:p.Glu202=
ENST00000563254.1:c.23G>A
ENST00000567787.1:c.*184G>A ENSP00000457251.1:n.*184G>A
NM_000326.4:c.606G>A NP_000317.1:p.Glu202=
XM_011521870.1:c.606G>A XP_011520172.1:p.Glu202=
XM_011521871.1:c.531G>A XP_011520173.1:p.Glu177=
XM_011521872.1:c.531G>A XP_011520174.1:p.Glu177=
XM_011521870.2:c.606G>A XP_011520172.1:p.Glu202=
XM_017022460.1:c.633G>A XP_016877949.1:p.Glu211=
NM_000326.5:c.606G>A MANE Select NP_000317.1:p.Glu202=