Canonical Allele Identifier: CA370568451
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs770829928
MyVariant Identifiers: chr8:g.23049299G>T (hg19) chr8:g.23191786G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191786G>T , CM000670.2:g.23191786G>T GRCh38
NC_000008.10:g.23049299G>T , CM000670.1:g.23049299G>T GRCh37
NC_000008.9:g.23105244G>T NCBI36
NG_032107.1:g.38382C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1315C>A MANE Select ENSP00000221132.3:p.His439Asn
ENST00000221132.7:c.1315C>A ENSP00000221132.3:p.His439Asn
ENST00000613472.1:c.841C>A ENSP00000480778.1:p.His281Asn
NM_003844.3:c.1315C>A NP_003835.3:p.His439Asn
NM_003844.4:c.1315C>A MANE Select NP_003835.3:p.His439Asn
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Search 100 bp 3'