Canonical Allele Identifier: CA118112
Gene: TNFRSF11A HGNC NCBI

Linked Data

ClinVar Variation Id: 6301
ClinVar RCV Id: RCV000006681
dbSNP Id: rs121908655
gnomAD v4: 18-62358328-A-G
MyVariant Identifiers: chr18:g.60025561A>G (hg19) chr18:g.62358328A>G (hg38)
PubMed: PMID:18606301 PMID:19940926
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.62358328A>G , CM000680.2:g.62358328A>G GRCh38
NC_000018.9:g.60025561A>G , CM000680.1:g.60025561A>G GRCh37
NC_000018.8:g.58176541A>G NCBI36
NG_008098.1:g.38014A>G , LRG_194:g.38014A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000586569.3:c.508A>G MANE Select ENSP00000465500.1:p.Arg170Gly
ENST00000639222.1:c.508A>G ENSP00000492422.1:p.Arg170Gly
ENST00000269485.11:c.508A>G ENSP00000269485.7:p.Arg170Gly
ENST00000586569.2:c.508A>G ENSP00000465500.1:p.Arg170Gly
ENST00000587697.1:n.426A>G
ENST00000616710.4:c.508A>G ENSP00000479567.1:p.Arg170Gly
ENST00000617039.4:c.508A>G ENSP00000482466.1:p.Arg170Gly
NM_001270949.1:c.508A>G NP_001257878.1:p.Arg170Gly
NM_001270950.1:c.508A>G NP_001257879.1:p.Arg170Gly
NM_001270951.1:c.508A>G NP_001257880.1:p.Arg170Gly
NM_001278268.1:c.466A>G NP_001265197.1:p.Arg156Gly
NM_003839.3:c.508A>G NP_003830.1:p.Arg170Gly
XM_011526244.1:c.523A>G XP_011524546.1:p.Arg175Gly
XM_011526245.1:c.400A>G XP_011524547.1:p.Arg134Gly
XR_935263.1:n.538A>G
XM_011526244.2:c.523A>G XP_011524546.1:p.Arg175Gly
XM_011526245.2:c.400A>G XP_011524547.1:p.Arg134Gly
XM_017026064.1:c.400A>G XP_016881553.1:p.Arg134Gly
XM_017026065.1:c.358A>G XP_016881554.1:p.Arg120Gly
XM_017026066.1:c.298A>G XP_016881555.1:p.Arg100Gly
NM_003839.4:c.508A>G MANE Select NP_003830.1:p.Arg170Gly
NM_001270951.2:c.508A>G NP_001257880.1:p.Arg170Gly
NM_001278268.2:c.466A>G NP_001265197.1:p.Arg156Gly
NM_001270949.2:c.508A>G NP_001257878.1:p.Arg170Gly
NM_001270950.2:c.508A>G NP_001257879.1:p.Arg170Gly
Search 100 bp 5'
Search 100 bp 3'