Canonical Allele Identifier: CA393729138

Gene: RLBP1

Linked Data

• dbSNP Id: rs1237226502
• gnomAD v2: 15-89755053-T-A
• gnomAD v4: 15-89211822-T-A
• MyVariant Identifiers: chr15:g.89755053T>A (hg19) ; chr15:g.89211822T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89211822T>A , CM000677.2:g.89211822T>A	GRCh38
NC_000015.9:g.89755053T>A , CM000677.1:g.89755053T>A	GRCh37
NC_000015.8:g.87556057T>A	NCBI36
NG_008116.1:g.14870A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268125.10:c.605A>T MANE Select	ENSP00000268125.5:p.Glu202Val
ENST00000268125.9:c.605A>T	ENSP00000268125.5:p.Glu202Val
ENST00000563254.1:c.22A>T
ENST00000567787.1:c.*183A>T	ENSP00000457251.1:n.*183A>T
NM_000326.4:c.605A>T	NP_000317.1:p.Glu202Val
XM_011521870.1:c.605A>T	XP_011520172.1:p.Glu202Val
XM_011521871.1:c.530A>T	XP_011520173.1:p.Glu177Val
XM_011521872.1:c.530A>T	XP_011520174.1:p.Glu177Val
XM_011521870.2:c.605A>T	XP_011520172.1:p.Glu202Val
XM_017022460.1:c.632A>T	XP_016877949.1:p.Glu211Val
NM_000326.5:c.605A>T MANE Select	NP_000317.1:p.Glu202Val