Canonical Allele Identifier: CA2573156427

Gene: RELB

Linked Data

• ClinVar Variation Id: 1541280
• ClinVar RCV Id: RCV002157388
• dbSNP Id: rs1971371513

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45012285G>C , CM000681.2:g.45012285G>C	GRCh38
NC_000019.9:g.45515543G>C , CM000681.1:g.45515543G>C	GRCh37
NC_000019.8:g.50207383G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505236.2:c.495+9G>C	ENSP00000423287.1:n.495+9G>C
ENST00000700471.1:c.342+9G>C	ENSP00000515004.1:n.342+9G>C
ENST00000221452.13:c.504+9G>C MANE Select	ENSP00000221452.7:n.504+9G>C
ENST00000221452.12:c.504+9G>C	ENSP00000221452.7:n.504+9G>C
ENST00000505236.1:c.495+9G>C	ENSP00000423287.1:n.495+9G>C
ENST00000625761.2:c.504+9G>C	ENSP00000485826.1:n.504+9G>C
NM_006509.3:c.504+9G>C	NP_006500.2:n.504+9G>C
XM_005259127.2:c.495+9G>C	XP_005259184.1:n.495+9G>C
XM_005259128.2:c.504+9G>C	XP_005259185.1:n.504+9G>C
XM_005259127.3:c.495+9G>C	XP_005259184.1:n.495+9G>C
NM_006509.4:c.504+9G>C MANE Select	NP_006500.2:n.504+9G>C