Canonical Allele Identifier: CA370568907
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23049358G>C (hg19) chr8:g.23191845G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191845G>C , CM000670.2:g.23191845G>C GRCh38
NC_000008.10:g.23049358G>C , CM000670.1:g.23049358G>C GRCh37
NC_000008.9:g.23105303G>C NCBI36
NG_032107.1:g.38323C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1256C>G MANE Select ENSP00000221132.3:p.Thr419Ser
ENST00000221132.7:c.1256C>G ENSP00000221132.3:p.Thr419Ser
ENST00000519862.1:n.311C>G
ENST00000613472.1:c.782C>G ENSP00000480778.1:p.Thr261Ser
NM_003844.3:c.1256C>G NP_003835.3:p.Thr419Ser
NM_003844.4:c.1256C>G MANE Select NP_003835.3:p.Thr419Ser
Search 100 bp 5'
Search 100 bp 3'