Canonical Allele Identifier: CA504078963

Gene: TNFRSF11A

Linked Data

• dbSNP Id: rs762733251
• gnomAD v2: 18-60027209-A-G
• gnomAD v3: 18-62359976-A-G
• gnomAD v4: 18-62359976-A-G
• MyVariant Identifiers: chr18:g.60027209A>G (hg19) ; chr18:g.62359976A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62359976A>G , CM000680.2:g.62359976A>G	GRCh38
NC_000018.9:g.60027209A>G , CM000680.1:g.60027209A>G	GRCh37
NC_000018.8:g.58178189A>G	NCBI36
NG_008098.1:g.39662A>G , LRG_194:g.39662A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.543A>G MANE Select	ENSP00000465500.1:p.Arg181=
ENST00000639222.1:c.543A>G	ENSP00000492422.1:p.Arg181=
ENST00000269485.11:c.543A>G	ENSP00000269485.7:p.Arg181=
ENST00000586569.2:c.543A>G	ENSP00000465500.1:p.Arg181=
ENST00000587697.1:n.461A>G
ENST00000616710.4:c.543A>G	ENSP00000479567.1:p.Arg181=
ENST00000617039.4:c.543A>G	ENSP00000482466.1:p.Arg181=
NM_001270949.1:c.543A>G	NP_001257878.1:p.Arg181=
NM_001270950.1:c.543A>G	NP_001257879.1:p.Arg181=
NM_001270951.1:c.543A>G	NP_001257880.1:p.Arg181=
NM_001278268.1:c.501A>G	NP_001265197.1:p.Arg167=
NM_003839.3:c.543A>G	NP_003830.1:p.Arg181=
XM_011526244.1:c.558A>G	XP_011524546.1:p.Arg186=
XM_011526245.1:c.435A>G	XP_011524547.1:p.Arg145=
XR_935263.1:n.573A>G
XM_011526244.2:c.558A>G	XP_011524546.1:p.Arg186=
XM_011526245.2:c.435A>G	XP_011524547.1:p.Arg145=
XM_017026064.1:c.435A>G	XP_016881553.1:p.Arg145=
XM_017026065.1:c.393A>G	XP_016881554.1:p.Arg131=
XM_017026066.1:c.333A>G	XP_016881555.1:p.Arg111=
NM_003839.4:c.543A>G MANE Select	NP_003830.1:p.Arg181=
NM_001270951.2:c.543A>G	NP_001257880.1:p.Arg181=
NM_001278268.2:c.501A>G	NP_001265197.1:p.Arg167=
NM_001270949.2:c.543A>G	NP_001257878.1:p.Arg181=
NM_001270950.2:c.543A>G	NP_001257879.1:p.Arg181=