Canonical Allele Identifier: CA15615238

Gene: TNFSF15

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114796423C>T , CM000671.2:g.114796423C>T	GRCh38
NC_000009.11:g.117558703C>T , CM000671.1:g.117558703C>T	GRCh37
NC_000009.10:g.116598524C>T	NCBI36
NG_011488.2:g.14706G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374045.5:c.211-2855G>A MANE Select	ENSP00000363157.3:n.211-2855G>A
ENST00000374045.4:c.211-2855G>A	ENSP00000363157.3:n.211-2855G>A
NM_005118.3:c.211-2855G>A	NP_005109.2:n.211-2855G>A
NM_005118.4:c.211-2855G>A MANE Select	NP_005109.2:n.211-2855G>A