Canonical Allele Identifier: CA2643342616

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12208409-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208409G>T , CM000663.2:g.12208409G>T	GRCh38
NC_000001.10:g.12268466G>T , CM000663.1:g.12268466G>T	GRCh37
NC_000001.9:g.12191053G>T	NCBI36
NG_029791.1:g.46407G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1389G>T MANE Select	ENSP00000365435.3:n.*1389G>T
ENST00000376259.6:c.*1389G>T	ENSP00000365435.3:n.*1389G>T
ENST00000492361.1:n.2764G>T
NM_001066.2:c.*1389G>T	NP_001057.1:n.*1389G>T
XM_011542060.1:c.*1389G>T	XP_011540362.1:n.*1389G>T
XM_011542061.1:c.*1389G>T	XP_011540363.1:n.*1389G>T
XM_011542062.1:c.2823G>T	XP_011540364.1:n.2823G>T
XM_011542063.1:c.*1389G>T	XP_011540365.1:n.*1389G>T
XM_011542060.2:c.*1389G>T	XP_011540362.1:n.*1389G>T
XM_011542063.2:c.*1389G>T	XP_011540365.1:n.*1389G>T
XM_017002214.1:c.*1389G>T	XP_016857703.1:n.*1389G>T
XM_017002215.1:c.*1389G>T	XP_016857704.1:n.*1389G>T
NM_001066.3:c.*1389G>T MANE Select	NP_001057.1:n.*1389G>T