Canonical Allele Identifier: CA370568924
Gene: TNFRSF10A HGNC NCBI

Linked Data

gnomAD v3: 8-23191846-T-C
gnomAD v4: 8-23191846-T-C
MyVariant Identifiers: chr8:g.23049359T>C (hg19) chr8:g.23191846T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191846T>C , CM000670.2:g.23191846T>C GRCh38
NC_000008.10:g.23049359T>C , CM000670.1:g.23049359T>C GRCh37
NC_000008.9:g.23105304T>C NCBI36
NG_032107.1:g.38322A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1255A>G MANE Select ENSP00000221132.3:p.Thr419Ala
ENST00000221132.7:c.1255A>G ENSP00000221132.3:p.Thr419Ala
ENST00000519862.1:n.310A>G
ENST00000613472.1:c.781A>G ENSP00000480778.1:p.Thr261Ala
NM_003844.3:c.1255A>G NP_003835.3:p.Thr419Ala
NM_003844.4:c.1255A>G MANE Select NP_003835.3:p.Thr419Ala
Search 100 bp 5'
Search 100 bp 3'