Canonical Allele Identifier: CA371920624
Gene: TNFRSF11B HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.119945289T>C (hg19) chr8:g.118933050T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933050T>C , CM000670.2:g.118933050T>C GRCh38
NC_000008.10:g.119945289T>C , CM000670.1:g.119945289T>C GRCh37
NC_000008.9:g.120014470T>C NCBI36
NG_012202.1:g.24095A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.281A>G MANE Select ENSP00000297350.4:p.Lys94Arg
ENST00000297350.8:c.281A>G ENSP00000297350.4:p.Lys94Arg
ENST00000517352.1:c.281A>G ENSP00000427924.1:p.Lys94Arg
NM_002546.3:c.281A>G NP_002537.3:p.Lys94Arg
NM_002546.4:c.281A>G MANE Select NP_002537.3:p.Lys94Arg
Search 100 bp 5'
Search 100 bp 3'