Canonical Allele Identifier: CA370576539
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23058220T>C (hg19) chr8:g.23200707T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23200707T>C , CM000670.2:g.23200707T>C GRCh38
NC_000008.10:g.23058220T>C , CM000670.1:g.23058220T>C GRCh37
NC_000008.9:g.23114165T>C NCBI36
NG_032107.1:g.29461A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.683A>G MANE Select ENSP00000221132.3:p.Glu228Gly
ENST00000221132.7:c.683A>G ENSP00000221132.3:p.Glu228Gly
ENST00000524158.5:c.77A>G ENSP00000428884.1:p.Glu26Gly
ENST00000613472.1:c.209A>G ENSP00000480778.1:p.Glu70Gly
NM_003844.3:c.683A>G NP_003835.3:p.Glu228Gly
NM_003844.4:c.683A>G MANE Select NP_003835.3:p.Glu228Gly
Search 100 bp 5'
Search 100 bp 3'