Canonical Allele Identifier: CA846345971

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs1295666115
• MyVariant Identifiers: chr8:g.119951697A>T (hg19) ; chr8:g.118939458A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118939458A>T , CM000670.2:g.118939458A>T	GRCh38
NC_000008.10:g.119951697A>T , CM000670.1:g.119951697A>T	GRCh37
NC_000008.9:g.120020878A>T	NCBI36
NG_012202.1:g.17687T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000297350.9:c.31-6158T>A MANE Select	ENSP00000297350.4:n.31-6158T>A
ENST00000297350.8:c.31-6158T>A	ENSP00000297350.4:n.31-6158T>A
ENST00000517352.1:c.31-6158T>A	ENSP00000427924.1:n.31-6158T>A
NM_002546.3:c.31-6158T>A	NP_002537.3:n.31-6158T>A
NM_002546.4:c.31-6158T>A MANE Select	NP_002537.3:n.31-6158T>A