Canonical Allele Identifier: CA8983786

Gene: TNFRSF11A

Linked Data

• ClinVar Variation Id: 259181
• ClinVar RCV Id: RCV000247457 ; RCV001668494
• dbSNP Id: rs6567271
• ExAC: 18:60027149 T / A
• gnomAD v2: 18-60027149-T-A
• gnomAD v3: 18-62359916-T-A
• gnomAD v4: 18-62359916-T-A
• MyVariant Identifiers: chr18:g.60027149T>A (hg19) ; chr18:g.62359916T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62359916T>A , CM000680.2:g.62359916T>A	GRCh38
NC_000018.9:g.60027149T>A , CM000680.1:g.60027149T>A	GRCh37
NC_000018.8:g.58178129T>A	NCBI36
NG_008098.1:g.39602T>A , LRG_194:g.39602T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.522-39T>A MANE Select	ENSP00000465500.1:n.522-39T>A
ENST00000639222.1:c.522-39T>A	ENSP00000492422.1:n.522-39T>A
ENST00000269485.11:c.522-39T>A	ENSP00000269485.7:n.522-39T>A
ENST00000586569.2:c.522-39T>A	ENSP00000465500.1:n.522-39T>A
ENST00000587697.1:n.440-39T>A
ENST00000616710.4:c.522-39T>A	ENSP00000479567.1:n.522-39T>A
ENST00000617039.4:c.522-39T>A	ENSP00000482466.1:n.522-39T>A
NM_001270949.1:c.522-39T>A	NP_001257878.1:n.522-39T>A
NM_001270950.1:c.522-39T>A	NP_001257879.1:n.522-39T>A
NM_001270951.1:c.522-39T>A	NP_001257880.1:n.522-39T>A
NM_001278268.1:c.480-39T>A	NP_001265197.1:n.480-39T>A
NM_003839.3:c.522-39T>A	NP_003830.1:n.522-39T>A
XM_011526244.1:c.537-39T>A	XP_011524546.1:n.537-39T>A
XM_011526245.1:c.414-39T>A	XP_011524547.1:n.414-39T>A
XR_935263.1:n.552-39T>A
XM_011526244.2:c.537-39T>A	XP_011524546.1:n.537-39T>A
XM_011526245.2:c.414-39T>A	XP_011524547.1:n.414-39T>A
XM_017026064.1:c.414-39T>A	XP_016881553.1:n.414-39T>A
XM_017026065.1:c.372-39T>A	XP_016881554.1:n.372-39T>A
XM_017026066.1:c.312-39T>A	XP_016881555.1:n.312-39T>A
NM_003839.4:c.522-39T>A MANE Select	NP_003830.1:n.522-39T>A
NM_001270951.2:c.522-39T>A	NP_001257880.1:n.522-39T>A
NM_001278268.2:c.480-39T>A	NP_001265197.1:n.480-39T>A
NM_001270949.2:c.522-39T>A	NP_001257878.1:n.522-39T>A
NM_001270950.2:c.522-39T>A	NP_001257879.1:n.522-39T>A