Canonical Allele Identifier: CA184865659
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs749780813
MyVariant Identifiers: chr8:g.119959820A>C (hg19) chr8:g.118947581A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118947581A>C , CM000670.2:g.118947581A>C GRCh38
NC_000008.10:g.119959820A>C , CM000670.1:g.119959820A>C GRCh37
NC_000008.9:g.120029001A>C NCBI36
NG_012202.1:g.9564T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297350.9:c.30+4211T>G MANE Select ENSP00000297350.4:n.30+4211T>G
ENST00000297350.8:c.30+4211T>G ENSP00000297350.4:n.30+4211T>G
ENST00000517352.1:c.30+4211T>G ENSP00000427924.1:n.30+4211T>G
NM_002546.3:c.30+4211T>G NP_002537.3:n.30+4211T>G
NM_002546.4:c.30+4211T>G MANE Select NP_002537.3:n.30+4211T>G
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