Canonical Allele Identifier: CA716899103

Gene: RLBP1

Linked Data

• dbSNP Id: rs1397529929
• gnomAD v3: 15-89211591-G-A
• gnomAD v4: 15-89211591-G-A
• MyVariant Identifiers: chr15:g.89754822G>A (hg19) ; chr15:g.89211591G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89211591G>A , CM000677.2:g.89211591G>A	GRCh38
NC_000015.9:g.89754822G>A , CM000677.1:g.89754822G>A	GRCh37
NC_000015.8:g.87555826G>A	NCBI36
NG_008116.1:g.15101C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268125.10:c.684+152C>T MANE Select	ENSP00000268125.5:n.684+152C>T
ENST00000268125.9:c.684+152C>T	ENSP00000268125.5:n.684+152C>T
ENST00000563254.1:c.101+152C>T
ENST00000567787.1:c.*262+152C>T	ENSP00000457251.1:n.*262+152C>T
NM_000326.4:c.684+152C>T	NP_000317.1:n.684+152C>T
XM_011521870.1:c.684+152C>T	XP_011520172.1:n.684+152C>T
XM_011521871.1:c.609+152C>T	XP_011520173.1:n.609+152C>T
XM_011521872.1:c.609+152C>T	XP_011520174.1:n.609+152C>T
XM_011521870.2:c.684+152C>T	XP_011520172.1:n.684+152C>T
XM_017022460.1:c.711+152C>T	XP_016877949.1:n.711+152C>T
NM_000326.5:c.684+152C>T MANE Select	NP_000317.1:n.684+152C>T