Canonical Allele Identifier: CA184864845

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs11573876
• gnomAD v2: 8-119951782-G-A
• gnomAD v3: 8-118939543-G-A
• gnomAD v4: 8-118939543-G-A
• MyVariant Identifiers: chr8:g.119951782G>A (hg19) ; chr8:g.118939543G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118939543G>A , CM000670.2:g.118939543G>A	GRCh38
NC_000008.10:g.119951782G>A , CM000670.1:g.119951782G>A	GRCh37
NC_000008.9:g.120020963G>A	NCBI36
NG_012202.1:g.17602C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000297350.9:c.31-6243C>T MANE Select	ENSP00000297350.4:n.31-6243C>T
ENST00000297350.8:c.31-6243C>T	ENSP00000297350.4:n.31-6243C>T
ENST00000517352.1:c.31-6243C>T	ENSP00000427924.1:n.31-6243C>T
NM_002546.3:c.31-6243C>T	NP_002537.3:n.31-6243C>T
NM_002546.4:c.31-6243C>T MANE Select	NP_002537.3:n.31-6243C>T