Canonical Allele Identifier: CA4674556
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs61761316
ExAC: 8:23049314 T / G
gnomAD v2: 8-23049314-T-G
gnomAD v3: 8-23191801-T-G
gnomAD v4: 8-23191801-T-G
MyVariant Identifiers: chr8:g.23049314T>G (hg19) chr8:g.23191801T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191801T>G , CM000670.2:g.23191801T>G GRCh38
NC_000008.10:g.23049314T>G , CM000670.1:g.23049314T>G GRCh37
NC_000008.9:g.23105259T>G NCBI36
NG_032107.1:g.38367A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1300A>C MANE Select ENSP00000221132.3:p.Arg434=
ENST00000221132.7:c.1300A>C ENSP00000221132.3:p.Arg434=
ENST00000613472.1:c.826A>C ENSP00000480778.1:p.Arg276=
NM_003844.3:c.1300A>C NP_003835.3:p.Arg434=
NM_003844.4:c.1300A>C MANE Select NP_003835.3:p.Arg434=
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