Canonical Allele Identifier: CA370568855
Gene: TNFRSF10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.23049350T>G (hg19) chr8:g.23191837T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191837T>G , CM000670.2:g.23191837T>G GRCh38
NC_000008.10:g.23049350T>G , CM000670.1:g.23049350T>G GRCh37
NC_000008.9:g.23105295T>G NCBI36
NG_032107.1:g.38331A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1264A>C MANE Select ENSP00000221132.3:p.Asn422His
ENST00000221132.7:c.1264A>C ENSP00000221132.3:p.Asn422His
ENST00000519862.1:n.319A>C
ENST00000613472.1:c.790A>C ENSP00000480778.1:p.Asn264His
NM_003844.3:c.1264A>C NP_003835.3:p.Asn422His
NM_003844.4:c.1264A>C MANE Select NP_003835.3:p.Asn422His
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Search 100 bp 3'