Canonical Allele Identifier: CA338455074

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252973C>G (hg19) ; chr1:g.12192916C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192916C>G , CM000663.2:g.12192916C>G	GRCh38
NC_000001.10:g.12252973C>G , CM000663.1:g.12252973C>G	GRCh37
NC_000001.9:g.12175560C>G	NCBI36
NG_029791.1:g.30914C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.605C>G MANE Select	ENSP00000365435.3:p.Ser202Cys
ENST00000376259.6:c.605C>G	ENSP00000365435.3:p.Ser202Cys
ENST00000489921.1:n.317C>G
ENST00000492361.1:n.594C>G
NM_001066.2:c.605C>G	NP_001057.1:p.Ser202Cys
XM_011542060.1:c.605C>G	XP_011540362.1:p.Ser202Cys
XM_011542061.1:c.605C>G	XP_011540363.1:p.Ser202Cys
XM_011542062.1:c.584C>G	XP_011540364.1:p.Ser195Cys
XM_011542063.1:c.605C>G	XP_011540365.1:p.Ser202Cys
XM_011542060.2:c.605C>G	XP_011540362.1:p.Ser202Cys
XM_011542063.2:c.605C>G	XP_011540365.1:p.Ser202Cys
XM_017002211.1:c.605C>G	XP_016857700.1:p.Ser202Cys
XM_017002214.1:c.20C>G	XP_016857703.1:p.Ser7Cys
XM_017002215.1:c.20C>G	XP_016857704.1:p.Ser7Cys
NM_001066.3:c.605C>G MANE Select	NP_001057.1:p.Ser202Cys