Canonical Allele Identifier: CA198898998
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1045193694
gnomAD v4: 9-114785329-C-T
MyVariant Identifiers: chr9:g.117547609C>T (hg19) chr9:g.114785329C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785329C>T , CM000671.2:g.114785329C>T GRCh38
NC_000009.11:g.117547609C>T , CM000671.1:g.117547609C>T GRCh37
NC_000009.10:g.116587430C>T NCBI36
NG_011488.2:g.25800G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5123G>A MANE Select ENSP00000363157.3:n.*5123G>A
ENST00000374045.4:c.*5123G>A ENSP00000363157.3:n.*5123G>A
NM_001204344.1:c.5702G>A NP_001191273.1:n.5702G>A
NM_005118.3:c.*5123G>A NP_005109.2:n.*5123G>A
NM_005118.4:c.*5123G>A MANE Select NP_005109.2:n.*5123G>A
Search 100 bp 5'
Search 100 bp 3'