Canonical Allele Identifier: CA2718210678
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs2129909608

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939513G>A , CM000670.2:g.118939513G>A GRCh38
NC_000008.10:g.119951752G>A , CM000670.1:g.119951752G>A GRCh37
NC_000008.9:g.120020933G>A NCBI36
NG_012202.1:g.17632C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.31-6213C>T MANE Select ENSP00000297350.4:n.31-6213C>T
ENST00000297350.8:c.31-6213C>T ENSP00000297350.4:n.31-6213C>T
ENST00000517352.1:c.31-6213C>T ENSP00000427924.1:n.31-6213C>T
NM_002546.3:c.31-6213C>T NP_002537.3:n.31-6213C>T
NM_002546.4:c.31-6213C>T MANE Select NP_002537.3:n.31-6213C>T