Canonical Allele Identifier: CA338455017

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252961C>G (hg19) ; chr1:g.12192904C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192904C>G , CM000663.2:g.12192904C>G	GRCh38
NC_000001.10:g.12252961C>G , CM000663.1:g.12252961C>G	GRCh37
NC_000001.9:g.12175548C>G	NCBI36
NG_029791.1:g.30902C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.593C>G MANE Select	ENSP00000365435.3:p.Ala198Gly
ENST00000376259.6:c.593C>G	ENSP00000365435.3:p.Ala198Gly
ENST00000489921.1:n.305C>G
ENST00000492361.1:n.582C>G
NM_001066.2:c.593C>G	NP_001057.1:p.Ala198Gly
XM_011542060.1:c.593C>G	XP_011540362.1:p.Ala198Gly
XM_011542061.1:c.593C>G	XP_011540363.1:p.Ala198Gly
XM_011542062.1:c.572C>G	XP_011540364.1:p.Ala191Gly
XM_011542063.1:c.593C>G	XP_011540365.1:p.Ala198Gly
XM_011542060.2:c.593C>G	XP_011540362.1:p.Ala198Gly
XM_011542063.2:c.593C>G	XP_011540365.1:p.Ala198Gly
XM_017002211.1:c.593C>G	XP_016857700.1:p.Ala198Gly
XM_017002214.1:c.8C>G	XP_016857703.1:p.Ala3Gly
XM_017002215.1:c.8C>G	XP_016857704.1:p.Ala3Gly
NM_001066.3:c.593C>G MANE Select	NP_001057.1:p.Ala198Gly