Canonical Allele Identifier: CA371920604
Gene: TNFRSF11B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933042A>G , CM000670.2:g.118933042A>G GRCh38
NC_000008.10:g.119945281A>G , CM000670.1:g.119945281A>G GRCh37
NC_000008.9:g.120014462A>G NCBI36
NG_012202.1:g.24103T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.289T>C MANE Select ENSP00000297350.4:p.Cys97Arg
ENST00000297350.8:c.289T>C ENSP00000297350.4:p.Cys97Arg
ENST00000517352.1:c.289T>C ENSP00000427924.1:p.Cys97Arg
NM_002546.3:c.289T>C NP_002537.3:p.Cys97Arg
NM_002546.4:c.289T>C MANE Select NP_002537.3:p.Cys97Arg