Canonical Allele Identifier: CA173931884
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs1028788152
gnomAD v4: 8-23191784-A-C
MyVariant Identifiers: chr8:g.23049297A>C (hg19) chr8:g.23191784A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191784A>C , CM000670.2:g.23191784A>C GRCh38
NC_000008.10:g.23049297A>C , CM000670.1:g.23049297A>C GRCh37
NC_000008.9:g.23105242A>C NCBI36
NG_032107.1:g.38384T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1317T>G MANE Select ENSP00000221132.3:p.His439Gln
ENST00000221132.7:c.1317T>G ENSP00000221132.3:p.His439Gln
ENST00000613472.1:c.843T>G ENSP00000480778.1:p.His281Gln
NM_003844.3:c.1317T>G NP_003835.3:p.His439Gln
NM_003844.4:c.1317T>G MANE Select NP_003835.3:p.His439Gln
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Search 100 bp 3'