Canonical Allele Identifier: CA198900160

Gene: TNFSF15

Linked Data

• dbSNP Id: rs1030924714
• gnomAD v2: 9-117558657-A-G
• gnomAD v3: 9-114796377-A-G
• gnomAD v4: 9-114796377-A-G
• MyVariant Identifiers: chr9:g.117558657A>G (hg19) ; chr9:g.114796377A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114796377A>G , CM000671.2:g.114796377A>G	GRCh38
NC_000009.11:g.117558657A>G , CM000671.1:g.117558657A>G	GRCh37
NC_000009.10:g.116598478A>G	NCBI36
NG_011488.2:g.14752T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374045.5:c.211-2809T>C MANE Select	ENSP00000363157.3:n.211-2809T>C
ENST00000374045.4:c.211-2809T>C	ENSP00000363157.3:n.211-2809T>C
NM_005118.3:c.211-2809T>C	NP_005109.2:n.211-2809T>C
NM_005118.4:c.211-2809T>C MANE Select	NP_005109.2:n.211-2809T>C