Canonical Allele Identifier: CA173956905
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1036448854
gnomAD v3: 8-23222709-T-C
gnomAD v4: 8-23222709-T-C
MyVariant Identifiers: chr8:g.23080222T>C (hg19) chr8:g.23222709T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222709T>C , CM000670.2:g.23222709T>C GRCh38
NC_000008.10:g.23080222T>C , CM000670.1:g.23080222T>C GRCh37
NC_000008.9:g.23136167T>C NCBI36
NG_032107.1:g.7459A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2047A>G MANE Select ENSP00000221132.3:n.306+2047A>G
ENST00000221132.7:c.306+2047A>G ENSP00000221132.3:n.306+2047A>G
ENST00000524158.5:c.-301+1724A>G ENSP00000428884.1:n.-301+1724A>G
ENST00000613472.1:c.31+2322A>G ENSP00000480778.1:n.31+2322A>G
NM_003844.3:c.306+2047A>G NP_003835.3:n.306+2047A>G
NM_003844.4:c.306+2047A>G MANE Select NP_003835.3:n.306+2047A>G
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