Canonical Allele Identifier: CA416364729

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252959T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192902T>C , CM000663.2:g.12192902T>C	GRCh38
NC_000001.10:g.12252959T>C , CM000663.1:g.12252959T>C	GRCh37
NC_000001.9:g.12175546T>C	NCBI36
NG_029791.1:g.30900T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.591T>C MANE Select	ENSP00000365435.3:p.Asp197=
ENST00000376259.6:c.591T>C	ENSP00000365435.3:p.Asp197=
ENST00000489921.1:n.303T>C
ENST00000492361.1:n.580T>C
NM_001066.2:c.591T>C	NP_001057.1:p.Asp197=
XM_011542060.1:c.591T>C	XP_011540362.1:p.Asp197=
XM_011542061.1:c.591T>C	XP_011540363.1:p.Asp197=
XM_011542062.1:c.570T>C	XP_011540364.1:p.Asp190=
XM_011542063.1:c.591T>C	XP_011540365.1:p.Asp197=
XM_011542060.2:c.591T>C	XP_011540362.1:p.Asp197=
XM_011542063.2:c.591T>C	XP_011540365.1:p.Asp197=
XM_017002211.1:c.591T>C	XP_016857700.1:p.Asp197=
XM_017002214.1:c.6T>C	XP_016857703.1:p.Asp2=
XM_017002215.1:c.6T>C	XP_016857704.1:p.Asp2=
NM_001066.3:c.591T>C MANE Select	NP_001057.1:p.Asp197=