Canonical Allele Identifier: CA462984371
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs780363937
gnomAD v3: 8-118933028-G-A
gnomAD v4: 8-118933028-G-A
MyVariant Identifiers: chr8:g.119945267G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933028G>A , CM000670.2:g.118933028G>A GRCh38
NC_000008.10:g.119945267G>A , CM000670.1:g.119945267G>A GRCh37
NC_000008.9:g.120014448G>A NCBI36
NG_012202.1:g.24117C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.303C>T MANE Select ENSP00000297350.4:p.His101=
ENST00000297350.8:c.303C>T ENSP00000297350.4:p.His101=
ENST00000517352.1:c.303C>T ENSP00000427924.1:p.His101=
NM_002546.3:c.303C>T NP_002537.3:p.His101=
NM_002546.4:c.303C>T MANE Select NP_002537.3:p.His101=
Search 100 bp 5'
Search 100 bp 3'