Canonical Allele Identifier: CA600834

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs201545665
• ExAC: 1:12252981 C / G
• gnomAD v2: 1-12252981-C-G
• gnomAD v3: 1-12192924-C-G
• gnomAD v4: 1-12192924-C-G
• MyVariant Identifiers: chr1:g.12252981C>G (hg19) ; chr1:g.12192924C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192924C>G , CM000663.2:g.12192924C>G	GRCh38
NC_000001.10:g.12252981C>G , CM000663.1:g.12252981C>G	GRCh37
NC_000001.9:g.12175568C>G	NCBI36
NG_029791.1:g.30922C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.613C>G MANE Select	ENSP00000365435.3:p.Pro205Ala
ENST00000376259.6:c.613C>G	ENSP00000365435.3:p.Pro205Ala
ENST00000489921.1:n.325C>G
ENST00000492361.1:n.602C>G
NM_001066.2:c.613C>G	NP_001057.1:p.Pro205Ala
XM_011542060.1:c.613C>G	XP_011540362.1:p.Pro205Ala
XM_011542061.1:c.613C>G	XP_011540363.1:p.Pro205Ala
XM_011542062.1:c.592C>G	XP_011540364.1:p.Pro198Ala
XM_011542063.1:c.613C>G	XP_011540365.1:p.Pro205Ala
XM_011542060.2:c.613C>G	XP_011540362.1:p.Pro205Ala
XM_011542063.2:c.613C>G	XP_011540365.1:p.Pro205Ala
XM_017002211.1:c.613C>G	XP_016857700.1:p.Pro205Ala
XM_017002214.1:c.28C>G	XP_016857703.1:p.Pro10Ala
XM_017002215.1:c.28C>G	XP_016857704.1:p.Pro10Ala
NM_001066.3:c.613C>G MANE Select	NP_001057.1:p.Pro205Ala