Canonical Allele Identifier: CA416364802

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12253055A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192998A>C , CM000663.2:g.12192998A>C	GRCh38
NC_000001.10:g.12253055A>C , CM000663.1:g.12253055A>C	GRCh37
NC_000001.9:g.12175642A>C	NCBI36
NG_029791.1:g.30996A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.687A>C MANE Select	ENSP00000365435.3:p.Pro229=
ENST00000376259.6:c.687A>C	ENSP00000365435.3:p.Pro229=
ENST00000489921.1:n.399A>C
ENST00000492361.1:n.676A>C
NM_001066.2:c.687A>C	NP_001057.1:p.Pro229=
XM_011542060.1:c.687A>C	XP_011540362.1:p.Pro229=
XM_011542061.1:c.687A>C	XP_011540363.1:p.Pro229=
XM_011542062.1:c.666A>C	XP_011540364.1:p.Pro222=
XM_011542063.1:c.687A>C	XP_011540365.1:p.Pro229=
XM_011542060.2:c.687A>C	XP_011540362.1:p.Pro229=
XM_011542063.2:c.687A>C	XP_011540365.1:p.Pro229=
XM_017002211.1:c.687A>C	XP_016857700.1:p.Pro229=
XM_017002214.1:c.102A>C	XP_016857703.1:p.Pro34=
XM_017002215.1:c.102A>C	XP_016857704.1:p.Pro34=
NM_001066.3:c.687A>C MANE Select	NP_001057.1:p.Pro229=