Canonical Allele Identifier: CA849995801
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1234895964
gnomAD v3: 8-23222495-A-G
gnomAD v4: 8-23222495-A-G
MyVariant Identifiers: chr8:g.23080008A>G (hg19) chr8:g.23222495A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222495A>G , CM000670.2:g.23222495A>G GRCh38
NC_000008.10:g.23080008A>G , CM000670.1:g.23080008A>G GRCh37
NC_000008.9:g.23135953A>G NCBI36
NG_032107.1:g.7673T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2261T>C MANE Select ENSP00000221132.3:n.306+2261T>C
ENST00000221132.7:c.306+2261T>C ENSP00000221132.3:n.306+2261T>C
ENST00000524158.5:c.-301+1938T>C ENSP00000428884.1:n.-301+1938T>C
ENST00000613472.1:c.31+2536T>C ENSP00000480778.1:n.31+2536T>C
NM_003844.3:c.306+2261T>C NP_003835.3:n.306+2261T>C
NM_003844.4:c.306+2261T>C MANE Select NP_003835.3:n.306+2261T>C
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