Canonical Allele Identifier: CA1874007113
Gene: TNFSF15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114804205G= , CM000671.2:g.114804205G= GRCh38
NC_000009.11:g.117566485G= , CM000671.1:g.117566485G= GRCh37
NC_000009.10:g.116606306G= NCBI36
NG_011488.2:g.6924C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.210+1598C= MANE Select ENSP00000363157.3:n.210+1598C=
ENST00000374045.4:c.210+1598C= ENSP00000363157.3:n.210+1598C=
NM_005118.3:c.210+1598C= NP_005109.2:n.210+1598C=
NM_005118.4:c.210+1598C= MANE Select NP_005109.2:n.210+1598C=
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