Canonical Allele Identifier: CA8983623

Gene: TNFRSF11A

Linked Data

• ClinVar Variation Id: 259177
• ClinVar RCV Id: RCV000249802 ; RCV000312036 ; RCV000370833 ; RCV001683040
• dbSNP Id: rs7238731
• ExAC: 18:59992547 G / A
• gnomAD v2: 18-59992547-G-A
• gnomAD v3: 18-62325314-G-A
• gnomAD v4: 18-62325314-G-A
• MyVariant Identifiers: chr18:g.59992547G>A (hg19) ; chr18:g.62325314G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62325314G>A , CM000680.2:g.62325314G>A	GRCh38
NC_000018.9:g.59992547G>A , CM000680.1:g.59992547G>A	GRCh37
NC_000018.8:g.58143527G>A	NCBI36
NG_008098.1:g.5000G>A , LRG_194:g.5000G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.-39G>A MANE Select	ENSP00000465500.1:n.-39G>A
ENST00000639222.1:c.-39G>A	ENSP00000492422.1:n.-39G>A
ENST00000269485.11:c.-39G>A	ENSP00000269485.7:n.-39G>A
ENST00000616710.4:c.-39G>A	ENSP00000479567.1:n.-39G>A
ENST00000617039.4:c.-39G>A	ENSP00000482466.1:n.-39G>A
NM_001270949.1:c.-39G>A	NP_001257878.1:n.-39G>A
NM_001270950.1:c.-39G>A	NP_001257879.1:n.-39G>A
NM_001270951.1:c.-39G>A	NP_001257880.1:n.-39G>A
NM_001278268.1:c.-39G>A	NP_001265197.1:n.-39G>A
NM_003839.3:c.-39G>A	NP_003830.1:n.-39G>A
NM_003839.4:c.-39G>A MANE Select	NP_003830.1:n.-39G>A
NM_001270951.2:c.-39G>A	NP_001257880.1:n.-39G>A
NM_001278268.2:c.-39G>A	NP_001265197.1:n.-39G>A
NM_001270949.2:c.-39G>A	NP_001257878.1:n.-39G>A
NM_001270950.2:c.-39G>A	NP_001257879.1:n.-39G>A