Canonical Allele Identifier: CA338455737

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12253045A>C (hg19) ; chr1:g.12192988A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192988A>C , CM000663.2:g.12192988A>C	GRCh38
NC_000001.10:g.12253045A>C , CM000663.1:g.12253045A>C	GRCh37
NC_000001.9:g.12175632A>C	NCBI36
NG_029791.1:g.30986A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.677A>C MANE Select	ENSP00000365435.3:p.His226Pro
ENST00000376259.6:c.677A>C	ENSP00000365435.3:p.His226Pro
ENST00000489921.1:n.389A>C
ENST00000492361.1:n.666A>C
NM_001066.2:c.677A>C	NP_001057.1:p.His226Pro
XM_011542060.1:c.677A>C	XP_011540362.1:p.His226Pro
XM_011542061.1:c.677A>C	XP_011540363.1:p.His226Pro
XM_011542062.1:c.656A>C	XP_011540364.1:p.His219Pro
XM_011542063.1:c.677A>C	XP_011540365.1:p.His226Pro
XM_011542060.2:c.677A>C	XP_011540362.1:p.His226Pro
XM_011542063.2:c.677A>C	XP_011540365.1:p.His226Pro
XM_017002211.1:c.677A>C	XP_016857700.1:p.His226Pro
XM_017002214.1:c.92A>C	XP_016857703.1:p.His31Pro
XM_017002215.1:c.92A>C	XP_016857704.1:p.His31Pro
NM_001066.3:c.677A>C MANE Select	NP_001057.1:p.His226Pro