Canonical Allele Identifier: CA338454914

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252927G>C (hg19) ; chr1:g.12192870G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192870G>C , CM000663.2:g.12192870G>C	GRCh38
NC_000001.10:g.12252927G>C , CM000663.1:g.12252927G>C	GRCh37
NC_000001.9:g.12175514G>C	NCBI36
NG_029791.1:g.30868G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.559G>C MANE Select	ENSP00000365435.3:p.Val187Leu
ENST00000376259.6:c.559G>C	ENSP00000365435.3:p.Val187Leu
ENST00000489921.1:n.271G>C
ENST00000492361.1:n.548G>C
NM_001066.2:c.559G>C	NP_001057.1:p.Val187Leu
XM_011542060.1:c.559G>C	XP_011540362.1:p.Val187Leu
XM_011542061.1:c.559G>C	XP_011540363.1:p.Val187Leu
XM_011542062.1:c.538G>C	XP_011540364.1:p.Val180Leu
XM_011542063.1:c.559G>C	XP_011540365.1:p.Val187Leu
XM_011542060.2:c.559G>C	XP_011540362.1:p.Val187Leu
XM_011542063.2:c.559G>C	XP_011540365.1:p.Val187Leu
XM_017002211.1:c.559G>C	XP_016857700.1:p.Val187Leu
XM_017002214.1:c.-27G>C	XP_016857703.1:n.-27G>C
XM_017002215.1:c.-27G>C	XP_016857704.1:n.-27G>C
NM_001066.3:c.559G>C MANE Select	NP_001057.1:p.Val187Leu