Canonical Allele Identifier: CA1814484897
Gene: TNFRSF11B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118952044G= , CM000670.2:g.118952044G= GRCh38
NC_000008.10:g.119964283G= , CM000670.1:g.119964283G= GRCh37
NC_000008.9:g.120033464G= NCBI36
NG_012202.1:g.5101C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.8:c.-223C= ENSP00000297350.4:n.-223C=
NM_002546.3:c.-223C= NP_002537.3:n.-223C=