Canonical Allele Identifier: CA600830
Gene: TNFRSF1B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1061622

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12192898T>G , CM000663.2:g.12192898T>G GRCh38
NC_000001.9:g.12175542T>G NCBI36
NC_000001.10:g.12252955T>G , CM000663.1:g.12252955T>G GRCh37
NG_029791.1:g.30896T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376259.6:c.587T>G ENSP00000365435.3:p.Met196Arg
ENST00000489921.1:n.299T>G
ENST00000492361.1:n.576T>G
NM_001066.2:c.587T>G VV NP_001057.1:p.Met196Arg
XM_011542060.1:c.587T>G XP_011540362.1:p.Met196Arg
XM_011542061.1:c.587T>G XP_011540363.1:p.Met196Arg
XM_011542062.1:n.566T>G XP_011540364.1:p.Met189Arg
XM_011542063.1:c.587T>G XP_011540365.1:p.Met196Arg