Canonical Allele Identifier: CA371920605
Gene: TNFRSF11B HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.289T>A MANE Select ENSP00000297350.4:p.Cys97Ser
ENST00000297350.8:c.289T>A ENSP00000297350.4:p.Cys97Ser
ENST00000517352.1:c.289T>A ENSP00000427924.1:p.Cys97Ser
NM_002546.3:c.289T>A NP_002537.3:p.Cys97Ser
NM_002546.4:c.289T>A MANE Select NP_002537.3:p.Cys97Ser