Canonical Allele Identifier: CA460179454
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23049378C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191865C>G , CM000670.2:g.23191865C>G GRCh38
NC_000008.10:g.23049378C>G , CM000670.1:g.23049378C>G GRCh37
NC_000008.9:g.23105323C>G NCBI36
NG_032107.1:g.38303G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1236G>C MANE Select ENSP00000221132.3:p.Leu412=
ENST00000221132.7:c.1236G>C ENSP00000221132.3:p.Leu412=
ENST00000519862.1:n.291G>C
ENST00000613472.1:c.762G>C ENSP00000480778.1:p.Leu254=
NM_003844.3:c.1236G>C NP_003835.3:p.Leu412=
NM_003844.4:c.1236G>C MANE Select NP_003835.3:p.Leu412=
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