Canonical Allele Identifier: CA1814477149
Gene: TNFRSF11B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939475T= , CM000670.2:g.118939475T= GRCh38
NC_000008.10:g.119951714T= , CM000670.1:g.119951714T= GRCh37
NC_000008.9:g.120020895T= NCBI36
NG_012202.1:g.17670A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.31-6175A= MANE Select ENSP00000297350.4:n.31-6175A=
ENST00000297350.8:c.31-6175A= ENSP00000297350.4:n.31-6175A=
ENST00000517352.1:c.31-6175A= ENSP00000427924.1:n.31-6175A=
NM_002546.3:c.31-6175A= NP_002537.3:n.31-6175A=
NM_002546.4:c.31-6175A= MANE Select NP_002537.3:n.31-6175A=