Canonical Allele Identifier: CA492076574
Gene: RLBP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.89755118A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89211887A>G , CM000677.2:g.89211887A>G GRCh38
NC_000015.9:g.89755118A>G , CM000677.1:g.89755118A>G GRCh37
NC_000015.8:g.87556122A>G NCBI36
NG_008116.1:g.14805T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000268125.10:c.540T>C MANE Select ENSP00000268125.5:p.Tyr180=
ENST00000268125.9:c.540T>C ENSP00000268125.5:p.Tyr180=
ENST00000567787.1:c.*118T>C ENSP00000457251.1:n.*118T>C
NM_000326.4:c.540T>C NP_000317.1:p.Tyr180=
XM_011521870.1:c.540T>C XP_011520172.1:p.Tyr180=
XM_011521871.1:c.465T>C XP_011520173.1:p.Tyr155=
XM_011521872.1:c.465T>C XP_011520174.1:p.Tyr155=
XM_011521870.2:c.540T>C XP_011520172.1:p.Tyr180=
XM_017022460.1:c.567T>C XP_016877949.1:p.Tyr189=
NM_000326.5:c.540T>C MANE Select NP_000317.1:p.Tyr180=