Canonical Allele Identifier: CA1874001379

Gene: TNFSF15

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114796480C= , CM000671.2:g.114796480C=	GRCh38
NC_000009.11:g.117558760C= , CM000671.1:g.117558760C=	GRCh37
NC_000009.10:g.116598581C=	NCBI36
NG_011488.2:g.14649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374045.5:c.211-2912G= MANE Select	ENSP00000363157.3:n.211-2912G=
ENST00000374045.4:c.211-2912G=	ENSP00000363157.3:n.211-2912G=
NM_005118.3:c.211-2912G=	NP_005109.2:n.211-2912G=
NM_005118.4:c.211-2912G= MANE Select	NP_005109.2:n.211-2912G=