Canonical Allele Identifier: CA1814477146
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1812448414

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939475_118939476del , CM000670.2:g.118939475_118939476del GRCh38
NC_000008.10:g.119951714_119951715del , CM000670.1:g.119951714_119951715del GRCh37
NC_000008.9:g.120020895_120020896del NCBI36
NG_012202.1:g.17671_17672del

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.31-6174_31-6173del MANE Select ENSP00000297350.4:n.31-6174_31-6173del
ENST00000297350.8:c.31-6174_31-6173del ENSP00000297350.4:n.31-6174_31-6173del
ENST00000517352.1:c.31-6174_31-6173del ENSP00000427924.1:n.31-6174_31-6173del
NM_002546.3:c.31-6174_31-6173del NP_002537.3:n.31-6174_31-6173del
NM_002546.4:c.31-6174_31-6173del MANE Select NP_002537.3:n.31-6174_31-6173del