Canonical Allele Identifier: CA849995808
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1331208929
MyVariant Identifiers: chr8:g.23080023C>T (hg19) chr8:g.23222510C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222510C>T , CM000670.2:g.23222510C>T GRCh38
NC_000008.10:g.23080023C>T , CM000670.1:g.23080023C>T GRCh37
NC_000008.9:g.23135968C>T NCBI36
NG_032107.1:g.7658G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.306+2246G>A MANE Select ENSP00000221132.3:n.306+2246G>A
ENST00000221132.7:c.306+2246G>A ENSP00000221132.3:n.306+2246G>A
ENST00000524158.5:c.-301+1923G>A ENSP00000428884.1:n.-301+1923G>A
ENST00000613472.1:c.31+2521G>A ENSP00000480778.1:n.31+2521G>A
NM_003844.3:c.306+2246G>A NP_003835.3:n.306+2246G>A
NM_003844.4:c.306+2246G>A MANE Select NP_003835.3:n.306+2246G>A
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