Canonical Allele Identifier: CA198900157

Gene: TNFSF15

Linked Data

• dbSNP Id: rs1003461001
• gnomAD v3: 9-114796332-C-T
• gnomAD v4: 9-114796332-C-T
• MyVariant Identifiers: chr9:g.117558612C>T (hg19) ; chr9:g.114796332C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114796332C>T , CM000671.2:g.114796332C>T	GRCh38
NC_000009.11:g.117558612C>T , CM000671.1:g.117558612C>T	GRCh37
NC_000009.10:g.116598433C>T	NCBI36
NG_011488.2:g.14797G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000374045.5:c.211-2764G>A MANE Select	ENSP00000363157.3:n.211-2764G>A
ENST00000374045.4:c.211-2764G>A	ENSP00000363157.3:n.211-2764G>A
NM_005118.3:c.211-2764G>A	NP_005109.2:n.211-2764G>A
NM_005118.4:c.211-2764G>A MANE Select	NP_005109.2:n.211-2764G>A