Canonical Allele Identifier: CA584549638
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs1211992021
gnomAD v2: 8-119945018-C-A
gnomAD v3: 8-118932779-C-A
gnomAD v4: 8-118932779-C-A
MyVariant Identifiers: chr8:g.119945018C>A (hg19) chr8:g.118932779C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118932779C>A , CM000670.2:g.118932779C>A GRCh38
NC_000008.10:g.119945018C>A , CM000670.1:g.119945018C>A GRCh37
NC_000008.9:g.120014199C>A NCBI36
NG_012202.1:g.24366G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.400+152G>T MANE Select ENSP00000297350.4:n.400+152G>T
ENST00000297350.8:c.400+152G>T ENSP00000297350.4:n.400+152G>T
ENST00000517352.1:c.400+152G>T ENSP00000427924.1:n.400+152G>T
NM_002546.3:c.400+152G>T NP_002537.3:n.400+152G>T
NM_002546.4:c.400+152G>T MANE Select NP_002537.3:n.400+152G>T
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