Canonical Allele Identifier: CA355537320
Gene: TNFSF10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172224311T>C (hg19) chr3:g.172506521T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172506521T>C , CM000665.2:g.172506521T>C GRCh38
NC_000003.11:g.172224311T>C , CM000665.1:g.172224311T>C GRCh37
NC_000003.10:g.173707005T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000241261.7:c.817A>G MANE Select ENSP00000241261.2:p.Ser273Gly
ENST00000241261.6:c.817A>G ENSP00000241261.2:p.Ser273Gly
ENST00000420541.6:c.*363A>G ENSP00000389931.2:n.*363A>G
NM_001190942.1:c.*363A>G NP_001177871.1:n.*363A>G
NM_003810.3:c.817A>G NP_003801.1:p.Ser273Gly
NR_033994.1:n.897A>G
NM_003810.4:c.817A>G MANE Select NP_003801.1:p.Ser273Gly
NM_001190942.2:c.*363A>G NP_001177871.1:n.*363A>G
NR_033994.2:n.820A>G
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