Canonical Allele Identifier: CA521207082

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1365378442
• gnomAD v2: 1-12268321-T-TAGCCATCTCTCTACTCCTACCTC
• gnomAD v3: 1-12208264-T-TAGCCATCTCTCTACTCCTACCTC
• gnomAD v4: 1-12208264-T-TAGCCATCTCTCTACTCCTACCTC
• MyVariant Identifiers: chr1:g.12268321_12268322insAGCCATCTCTCTACTCCTACCTC (hg19) ; chr1:g.12208264_12208265insAGCCATCTCTCTACTCCTACCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208269_12208291dup , CM000663.2:g.12208269_12208291dup	GRCh38
NC_000001.10:g.12268326_12268348dup , CM000663.1:g.12268326_12268348dup	GRCh37
NC_000001.9:g.12190913_12190935dup	NCBI36
NG_029791.1:g.46267_46289dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.*1249_*1271dup MANE Select	ENSP00000365435.3:n.*1249_*1271dup
ENST00000376259.6:c.*1249_*1271dup	ENSP00000365435.3:n.*1249_*1271dup
ENST00000492361.1:n.2624_2646dup
NM_001066.2:c.*1249_*1271dup	NP_001057.1:n.*1249_*1271dup
XM_011542060.1:c.*1249_*1271dup	XP_011540362.1:n.*1249_*1271dup
XM_011542061.1:c.*1249_*1271dup	XP_011540363.1:n.*1249_*1271dup
XM_011542062.1:c.2683_2705dup	XP_011540364.1:n.2683_2705dup
XM_011542063.1:c.*1249_*1271dup	XP_011540365.1:n.*1249_*1271dup
XM_011542060.2:c.*1249_*1271dup	XP_011540362.1:n.*1249_*1271dup
XM_011542063.2:c.*1249_*1271dup	XP_011540365.1:n.*1249_*1271dup
XM_017002214.1:c.*1249_*1271dup	XP_016857703.1:n.*1249_*1271dup
XM_017002215.1:c.*1249_*1271dup	XP_016857704.1:n.*1249_*1271dup
NM_001066.3:c.*1249_*1271dup MANE Select	NP_001057.1:n.*1249_*1271dup