Canonical Allele Identifier: CA198900159
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs746773645
MyVariant Identifiers: chr9:g.117558643T>G (hg19) chr9:g.114796363T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796363T>G , CM000671.2:g.114796363T>G GRCh38
NC_000009.11:g.117558643T>G , CM000671.1:g.117558643T>G GRCh37
NC_000009.10:g.116598464T>G NCBI36
NG_011488.2:g.14766A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.211-2795A>C MANE Select ENSP00000363157.3:n.211-2795A>C
ENST00000374045.4:c.211-2795A>C ENSP00000363157.3:n.211-2795A>C
NM_005118.3:c.211-2795A>C NP_005109.2:n.211-2795A>C
NM_005118.4:c.211-2795A>C MANE Select NP_005109.2:n.211-2795A>C
Search 100 bp 5'
Search 100 bp 3'