Canonical Allele Identifier: CA371920654
Gene: TNFRSF11B HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.119945302G>T (hg19) chr8:g.118933063G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933063G>T , CM000670.2:g.118933063G>T GRCh38
NC_000008.10:g.119945302G>T , CM000670.1:g.119945302G>T GRCh37
NC_000008.9:g.120014483G>T NCBI36
NG_012202.1:g.24082C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.268C>A MANE Select ENSP00000297350.4:p.Leu90Met
ENST00000297350.8:c.268C>A ENSP00000297350.4:p.Leu90Met
ENST00000517352.1:c.268C>A ENSP00000427924.1:p.Leu90Met
NM_002546.3:c.268C>A NP_002537.3:p.Leu90Met
NM_002546.4:c.268C>A MANE Select NP_002537.3:p.Leu90Met
Search 100 bp 5'
Search 100 bp 3'