Canonical Allele Identifier: CA4674954
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs144035000
ExAC: 8:23069691 T / C
gnomAD v2: 8-23069691-T-C
gnomAD v3: 8-23212178-T-C
gnomAD v4: 8-23212178-T-C
MyVariant Identifiers: chr8:g.23069691T>C (hg19) chr8:g.23212178T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212178T>C , CM000670.2:g.23212178T>C GRCh38
NC_000008.10:g.23069691T>C , CM000670.1:g.23069691T>C GRCh37
NC_000008.9:g.23125636T>C NCBI36
NG_032107.1:g.17990A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.341A>G MANE Select ENSP00000221132.3:p.His114Arg
ENST00000221132.7:c.341A>G ENSP00000221132.3:p.His114Arg
ENST00000524158.5:c.-266A>G ENSP00000428884.1:n.-266A>G
ENST00000613472.1:c.32-9519A>G ENSP00000480778.1:n.32-9519A>G
NM_003844.3:c.341A>G NP_003835.3:p.His114Arg
NM_003844.4:c.341A>G MANE Select NP_003835.3:p.His114Arg
Search 100 bp 5'
Search 100 bp 3'