Canonical Allele Identifier: CA1814477156
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1812448537

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118939486G>A , CM000670.2:g.118939486G>A GRCh38
NC_000008.10:g.119951725G>A , CM000670.1:g.119951725G>A GRCh37
NC_000008.9:g.120020906G>A NCBI36
NG_012202.1:g.17659C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.31-6186C>T MANE Select ENSP00000297350.4:n.31-6186C>T
ENST00000297350.8:c.31-6186C>T ENSP00000297350.4:n.31-6186C>T
ENST00000517352.1:c.31-6186C>T ENSP00000427924.1:n.31-6186C>T
NM_002546.3:c.31-6186C>T NP_002537.3:n.31-6186C>T
NM_002546.4:c.31-6186C>T MANE Select NP_002537.3:n.31-6186C>T