Canonical Allele Identifier: CA10648054
Gene: TNFRSF11A HGNC NCBI

Linked Data

ClinVar Variation Id: 327723
ClinVar RCV Id: RCV000275612 RCV000356202
dbSNP Id: rs886054081
gnomAD v2: 18-59992537-G-A
gnomAD v3: 18-62325304-G-A
gnomAD v4: 18-62325304-G-A
MyVariant Identifiers: chr18:g.59992537G>A (hg19) chr18:g.62325304G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.62325304G>A , CM000680.2:g.62325304G>A GRCh38
NC_000018.9:g.59992537G>A , CM000680.1:g.59992537G>A GRCh37
NC_000018.8:g.58143517G>A NCBI36
NG_008098.1:g.4990G>A , LRG_194:g.4990G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000639222.1:c.-49G>A ENSP00000492422.1:n.-49G>A
ENST00000269485.11:c.-49G>A ENSP00000269485.7:n.-49G>A
ENST00000616710.4:c.-49G>A ENSP00000479567.1:n.-49G>A
ENST00000617039.4:c.-49G>A ENSP00000482466.1:n.-49G>A
NM_001270949.1:c.-49G>A NP_001257878.1:n.-49G>A
NM_001270950.1:c.-49G>A NP_001257879.1:n.-49G>A
NM_001270951.1:c.-49G>A NP_001257880.1:n.-49G>A
NM_001278268.1:c.-49G>A NP_001265197.1:n.-49G>A
NM_003839.3:c.-49G>A NP_003830.1:n.-49G>A
Search 100 bp 5'
Search 100 bp 3'