Canonical Allele Identifier: CA1874001235
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796289G= , CM000671.2:g.114796289G= GRCh38
NC_000009.11:g.117558569G= , CM000671.1:g.117558569G= GRCh37
NC_000009.10:g.116598390G= NCBI36
NG_011488.2:g.14840C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2721C= MANE Select ENSP00000363157.3:n.211-2721C=
ENST00000374045.4:c.211-2721C= ENSP00000363157.3:n.211-2721C=
NM_005118.3:c.211-2721C= NP_005109.2:n.211-2721C=
NM_005118.4:c.211-2721C= MANE Select NP_005109.2:n.211-2721C=