Canonical Allele Identifier: CA338455006

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12192902-T-A
• MyVariant Identifiers: chr1:g.12252959T>A (hg19) ; chr1:g.12192902T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192902T>A , CM000663.2:g.12192902T>A	GRCh38
NC_000001.10:g.12252959T>A , CM000663.1:g.12252959T>A	GRCh37
NC_000001.9:g.12175546T>A	NCBI36
NG_029791.1:g.30900T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.591T>A MANE Select	ENSP00000365435.3:p.Asp197Glu
ENST00000376259.6:c.591T>A	ENSP00000365435.3:p.Asp197Glu
ENST00000489921.1:n.303T>A
ENST00000492361.1:n.580T>A
NM_001066.2:c.591T>A	NP_001057.1:p.Asp197Glu
XM_011542060.1:c.591T>A	XP_011540362.1:p.Asp197Glu
XM_011542061.1:c.591T>A	XP_011540363.1:p.Asp197Glu
XM_011542062.1:c.570T>A	XP_011540364.1:p.Asp190Glu
XM_011542063.1:c.591T>A	XP_011540365.1:p.Asp197Glu
XM_011542060.2:c.591T>A	XP_011540362.1:p.Asp197Glu
XM_011542063.2:c.591T>A	XP_011540365.1:p.Asp197Glu
XM_017002211.1:c.591T>A	XP_016857700.1:p.Asp197Glu
XM_017002214.1:c.6T>A	XP_016857703.1:p.Asp2Glu
XM_017002215.1:c.6T>A	XP_016857704.1:p.Asp2Glu
NM_001066.3:c.591T>A MANE Select	NP_001057.1:p.Asp197Glu