Canonical Allele Identifier: CA370568696
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1800758177
MyVariant Identifiers: chr8:g.23049332G>C (hg19) chr8:g.23191819G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191819G>C , CM000670.2:g.23191819G>C GRCh38
NC_000008.10:g.23049332G>C , CM000670.1:g.23049332G>C GRCh37
NC_000008.9:g.23105277G>C NCBI36
NG_032107.1:g.38349C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1282C>G MANE Select ENSP00000221132.3:p.Leu428Val
ENST00000221132.7:c.1282C>G ENSP00000221132.3:p.Leu428Val
ENST00000519862.1:n.337C>G
ENST00000613472.1:c.808C>G ENSP00000480778.1:p.Leu270Val
NM_003844.3:c.1282C>G NP_003835.3:p.Leu428Val
NM_003844.4:c.1282C>G MANE Select NP_003835.3:p.Leu428Val
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