Canonical Allele Identifier: CA1814477179

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs1812448890

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118939512A>G , CM000670.2:g.118939512A>G	GRCh38
NC_000008.10:g.119951751A>G , CM000670.1:g.119951751A>G	GRCh37
NC_000008.9:g.120020932A>G	NCBI36
NG_012202.1:g.17633T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000297350.9:c.31-6212T>C MANE Select	ENSP00000297350.4:n.31-6212T>C
ENST00000297350.8:c.31-6212T>C	ENSP00000297350.4:n.31-6212T>C
ENST00000517352.1:c.31-6212T>C	ENSP00000427924.1:n.31-6212T>C
NM_002546.3:c.31-6212T>C	NP_002537.3:n.31-6212T>C
NM_002546.4:c.31-6212T>C MANE Select	NP_002537.3:n.31-6212T>C