Canonical Allele Identifier: CA198898997

Gene: TNFSF15

Linked Data

• dbSNP Id: rs946470607
• gnomAD v2: 9-117547596-A-G
• gnomAD v3: 9-114785316-A-G
• gnomAD v4: 9-114785316-A-G
• MyVariant Identifiers: chr9:g.117547596A>G (hg19) ; chr9:g.114785316A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114785316A>G , CM000671.2:g.114785316A>G	GRCh38
NC_000009.11:g.117547596A>G , CM000671.1:g.117547596A>G	GRCh37
NC_000009.10:g.116587417A>G	NCBI36
NG_011488.2:g.25813T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374045.5:c.*5136T>C MANE Select	ENSP00000363157.3:n.*5136T>C
ENST00000374045.4:c.*5136T>C	ENSP00000363157.3:n.*5136T>C
NM_001204344.1:c.5715T>C	NP_001191273.1:n.5715T>C
NM_005118.3:c.*5136T>C	NP_005109.2:n.*5136T>C
NM_005118.4:c.*5136T>C MANE Select	NP_005109.2:n.*5136T>C