Canonical Allele Identifier: CA4674559
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs373461559
ExAC: 8:23049331 A / G
gnomAD v2: 8-23049331-A-G
gnomAD v3: 8-23191818-A-G
gnomAD v4: 8-23191818-A-G
MyVariant Identifiers: chr8:g.23049331A>G (hg19) chr8:g.23191818A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191818A>G , CM000670.2:g.23191818A>G GRCh38
NC_000008.10:g.23049331A>G , CM000670.1:g.23049331A>G GRCh37
NC_000008.9:g.23105276A>G NCBI36
NG_032107.1:g.38350T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1283T>C MANE Select ENSP00000221132.3:p.Leu428Pro
ENST00000221132.7:c.1283T>C ENSP00000221132.3:p.Leu428Pro
ENST00000519862.1:n.338T>C
ENST00000613472.1:c.809T>C ENSP00000480778.1:p.Leu270Pro
NM_003844.3:c.1283T>C NP_003835.3:p.Leu428Pro
NM_003844.4:c.1283T>C MANE Select NP_003835.3:p.Leu428Pro
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