Canonical Allele Identifier: CA436970386
Gene: TNFSF10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172224312G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172506522G>T , CM000665.2:g.172506522G>T GRCh38
NC_000003.11:g.172224312G>T , CM000665.1:g.172224312G>T GRCh37
NC_000003.10:g.173707006G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000241261.7:c.816C>A MANE Select ENSP00000241261.2:p.Ala272=
ENST00000241261.6:c.816C>A ENSP00000241261.2:p.Ala272=
ENST00000420541.6:c.*362C>A ENSP00000389931.2:n.*362C>A
NM_001190942.1:c.*362C>A NP_001177871.1:n.*362C>A
NM_003810.3:c.816C>A NP_003801.1:p.Ala272=
NR_033994.1:n.896C>A
NM_003810.4:c.816C>A MANE Select NP_003801.1:p.Ala272=
NM_001190942.2:c.*362C>A NP_001177871.1:n.*362C>A
NR_033994.2:n.819C>A
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