Canonical Allele Identifier: CA2580097380

Gene: RELB

Linked Data

• ClinVar Variation Id: 2108321
• ClinVar RCV Id: RCV003034118

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45002999G>T , CM000681.2:g.45002999G>T	GRCh38
NC_000019.9:g.45506257G>T , CM000681.1:g.45506257G>T	GRCh37
NC_000019.8:g.50198097G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505236.2:c.154+3G>T	ENSP00000423287.1:n.154+3G>T
ENST00000221452.13:c.154+3G>T MANE Select	ENSP00000221452.7:n.154+3G>T
ENST00000221452.12:c.154+3G>T	ENSP00000221452.7:n.154+3G>T
ENST00000505236.1:c.154+3G>T	ENSP00000423287.1:n.154+3G>T
ENST00000509480.5:c.154+3G>T	ENSP00000427348.1:n.154+3G>T
ENST00000625761.2:c.152+5G>T	ENSP00000485826.1:n.152+5G>T
NM_006509.3:c.154+3G>T	NP_006500.2:n.154+3G>T
XM_005259127.2:c.154+3G>T	XP_005259184.1:n.154+3G>T
XM_005259128.2:c.154+3G>T	XP_005259185.1:n.154+3G>T
XM_005259127.3:c.154+3G>T	XP_005259184.1:n.154+3G>T
NM_006509.4:c.154+3G>T MANE Select	NP_006500.2:n.154+3G>T