Canonical Allele Identifier: CA590281545

Gene: TNFSF15

Linked Data

• dbSNP Id: rs1380561016
• gnomAD v2: 9-117547594-T-A
• gnomAD v3: 9-114785314-T-A
• gnomAD v4: 9-114785314-T-A
• MyVariant Identifiers: chr9:g.117547594T>A (hg19) ; chr9:g.114785314T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114785314T>A , CM000671.2:g.114785314T>A	GRCh38
NC_000009.11:g.117547594T>A , CM000671.1:g.117547594T>A	GRCh37
NC_000009.10:g.116587415T>A	NCBI36
NG_011488.2:g.25815A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374045.5:c.*5138A>T MANE Select	ENSP00000363157.3:n.*5138A>T
ENST00000374045.4:c.*5138A>T	ENSP00000363157.3:n.*5138A>T
NM_001204344.1:c.5717A>T	NP_001191273.1:n.5717A>T
NM_005118.3:c.*5138A>T	NP_005109.2:n.*5138A>T
NM_005118.4:c.*5138A>T MANE Select	NP_005109.2:n.*5138A>T