Canonical Allele Identifier: CA371920655
Gene: TNFRSF11B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933064C>A , CM000670.2:g.118933064C>A GRCh38
NC_000008.10:g.119945303C>A , CM000670.1:g.119945303C>A GRCh37
NC_000008.9:g.120014484C>A NCBI36
NG_012202.1:g.24081G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.267G>T MANE Select ENSP00000297350.4:p.Glu89Asp
ENST00000297350.8:c.267G>T ENSP00000297350.4:p.Glu89Asp
ENST00000517352.1:c.267G>T ENSP00000427924.1:p.Glu89Asp
NM_002546.3:c.267G>T NP_002537.3:p.Glu89Asp
NM_002546.4:c.267G>T MANE Select NP_002537.3:p.Glu89Asp