Canonical Allele Identifier: CA1874001226
Gene: TNFSF15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796262C= , CM000671.2:g.114796262C= GRCh38
NC_000009.11:g.117558542C= , CM000671.1:g.117558542C= GRCh37
NC_000009.10:g.116598363C= NCBI36
NG_011488.2:g.14867G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2694G= MANE Select ENSP00000363157.3:n.211-2694G=
ENST00000374045.4:c.211-2694G= ENSP00000363157.3:n.211-2694G=
NM_005118.3:c.211-2694G= NP_005109.2:n.211-2694G=
NM_005118.4:c.211-2694G= MANE Select NP_005109.2:n.211-2694G=
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