Canonical Allele Identifier: CA198900147
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs961234744
MyVariant Identifiers: chr9:g.114796240G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796240G>T , CM000671.2:g.114796240G>T GRCh38
NC_000009.11:g.117558520G>T , CM000671.1:g.117558520G>T GRCh37
NC_000009.10:g.116598341G>T NCBI36
NG_011488.2:g.14889C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2672C>A MANE Select ENSP00000363157.3:n.211-2672C>A
ENST00000374045.4:c.211-2672C>A ENSP00000363157.3:n.211-2672C>A
NM_005118.3:c.211-2672C>A NP_005109.2:n.211-2672C>A
NM_005118.4:c.211-2672C>A MANE Select NP_005109.2:n.211-2672C>A
Search 100 bp 5'
Search 100 bp 3'