Canonical Allele Identifier: CA459967847
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23069708A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212195A>C , CM000670.2:g.23212195A>C GRCh38
NC_000008.10:g.23069708A>C , CM000670.1:g.23069708A>C GRCh37
NC_000008.9:g.23125653A>C NCBI36
NG_032107.1:g.17973T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.324T>G MANE Select ENSP00000221132.3:p.Ala108=
ENST00000221132.7:c.324T>G ENSP00000221132.3:p.Ala108=
ENST00000524158.5:c.-283T>G ENSP00000428884.1:n.-283T>G
ENST00000613472.1:c.32-9536T>G ENSP00000480778.1:n.32-9536T>G
NM_003844.3:c.324T>G NP_003835.3:p.Ala108=
NM_003844.4:c.324T>G MANE Select NP_003835.3:p.Ala108=
Search 100 bp 5'
Search 100 bp 3'