Canonical Allele Identifier: CA338456067

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12193024-G-C
• MyVariant Identifiers: chr1:g.12253081G>C (hg19) ; chr1:g.12193024G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12193024G>C , CM000663.2:g.12193024G>C	GRCh38
NC_000001.10:g.12253081G>C , CM000663.1:g.12253081G>C	GRCh37
NC_000001.9:g.12175668G>C	NCBI36
NG_029791.1:g.31022G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.713G>C MANE Select	ENSP00000365435.3:p.Ser238Thr
ENST00000376259.6:c.713G>C	ENSP00000365435.3:p.Ser238Thr
ENST00000492361.1:n.702G>C
NM_001066.2:c.713G>C	NP_001057.1:p.Ser238Thr
XM_011542060.1:c.713G>C	XP_011540362.1:p.Ser238Thr
XM_011542061.1:c.713G>C	XP_011540363.1:p.Ser238Thr
XM_011542062.1:c.692G>C	XP_011540364.1:p.Ser231Thr
XM_011542063.1:c.713G>C	XP_011540365.1:p.Ser238Thr
XM_011542060.2:c.713G>C	XP_011540362.1:p.Ser238Thr
XM_011542063.2:c.713G>C	XP_011540365.1:p.Ser238Thr
XM_017002211.1:c.713G>C	XP_016857700.1:p.Ser238Thr
XM_017002214.1:c.128G>C	XP_016857703.1:p.Ser43Thr
XM_017002215.1:c.128G>C	XP_016857704.1:p.Ser43Thr
NM_001066.3:c.713G>C MANE Select	NP_001057.1:p.Ser238Thr