Canonical Allele Identifier: CA1874001225
Gene: TNFSF15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796261C= , CM000671.2:g.114796261C= GRCh38
NC_000009.11:g.117558541C= , CM000671.1:g.117558541C= GRCh37
NC_000009.10:g.116598362C= NCBI36
NG_011488.2:g.14868G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2693G= MANE Select ENSP00000363157.3:n.211-2693G=
ENST00000374045.4:c.211-2693G= ENSP00000363157.3:n.211-2693G=
NM_005118.3:c.211-2693G= NP_005109.2:n.211-2693G=
NM_005118.4:c.211-2693G= MANE Select NP_005109.2:n.211-2693G=
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