Canonical Allele Identifier: CA370568885
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1274131618
gnomAD v2: 8-23049355-C-T
gnomAD v3: 8-23191842-C-T
gnomAD v4: 8-23191842-C-T
MyVariant Identifiers: chr8:g.23049355C>T (hg19) chr8:g.23191842C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191842C>T , CM000670.2:g.23191842C>T GRCh38
NC_000008.10:g.23049355C>T , CM000670.1:g.23049355C>T GRCh37
NC_000008.9:g.23105300C>T NCBI36
NG_032107.1:g.38326G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1259G>A MANE Select ENSP00000221132.3:p.Gly420Glu
ENST00000221132.7:c.1259G>A ENSP00000221132.3:p.Gly420Glu
ENST00000519862.1:n.314G>A
ENST00000613472.1:c.785G>A ENSP00000480778.1:p.Gly262Glu
NM_003844.3:c.1259G>A NP_003835.3:p.Gly420Glu
NM_003844.4:c.1259G>A MANE Select NP_003835.3:p.Gly420Glu
Search 100 bp 5'
Search 100 bp 3'