Canonical Allele Identifier: CA370569442

Gene: RHOBTB2 TNFRSF10B

Linked Data

• ClinVar Variation Id: 495261
• ClinVar RCV Id: RCV000585816 ; RCV001266474 ; RCV000656374 ; RCV001090302
• dbSNP Id: rs1554504681
• MyVariant Identifiers: chr8:g.22865223C>T (hg19) ; chr8:g.23007710C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23007710C>T , CM000670.2:g.23007710C>T	GRCh38
NC_000008.10:g.22865223C>T , CM000670.1:g.22865223C>T	GRCh37
NC_000008.9:g.22921168C>T	NCBI36
NG_047133.1:g.25453C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692529.1:c.1492C>T (RHOBTB2)	ENSP00000509630.1:p.Arg498Trp
ENST00000251822.7:c.1465C>T (RHOBTB2) MANE Select	ENSP00000251822.7:p.Arg489Trp
ENST00000251822.6:c.1465C>T (RHOBTB2)	ENSP00000251822.6:p.Arg489Trp
ENST00000519685.5:c.1531C>T (RHOBTB2)	ENSP00000427926.1:p.Arg511Trp
ENST00000522948.5:c.1486C>T (RHOBTB2)	ENSP00000429141.1:p.Arg496Trp
NM_001160036.1:c.1531C>T (RHOBTB2)	NP_001153508.1:p.Arg511Trp
NM_001160037.1:c.1486C>T (RHOBTB2)	NP_001153509.1:p.Arg496Trp
NM_015178.2:c.1465C>T (RHOBTB2)	NP_055993.2:p.Arg489Trp
XM_006716315.2:c.1531C>T (RHOBTB2)	XP_006716378.1:p.Arg511Trp
XM_011544454.1:c.1543C>T (RHOBTB2)	XP_011542756.1:p.Arg515Trp
XR_949500.1:n.5567G>A (TNFRSF10B)
XM_017013251.1:c.1531C>T (RHOBTB2)	XP_016868740.1:p.Arg511Trp
NM_001160036.2:c.1531C>T (RHOBTB2)	NP_001153508.1:p.Arg511Trp
NM_001160037.2:c.1486C>T (RHOBTB2)	NP_001153509.1:p.Arg496Trp
NM_001374791.1:c.1465C>T (RHOBTB2)	NP_001361720.1:p.Arg489Trp
NM_015178.3:c.1465C>T (RHOBTB2) MANE Select	NP_055993.2:p.Arg489Trp