Canonical Allele Identifier: CA1814477159
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1812448570

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939488dup , CM000670.2:g.118939488dup GRCh38
NC_000008.10:g.119951727dup , CM000670.1:g.119951727dup GRCh37
NC_000008.9:g.120020908dup NCBI36
NG_012202.1:g.17657dup

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.31-6188dup MANE Select ENSP00000297350.4:n.31-6188dup
ENST00000297350.8:c.31-6188dup ENSP00000297350.4:n.31-6188dup
ENST00000517352.1:c.31-6188dup ENSP00000427924.1:n.31-6188dup
NM_002546.3:c.31-6188dup NP_002537.3:n.31-6188dup
NM_002546.4:c.31-6188dup MANE Select NP_002537.3:n.31-6188dup