Canonical Allele Identifier: CA1874007055

Gene: TNFSF15

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114804113A= , CM000671.2:g.114804113A=	GRCh38
NC_000009.11:g.117566393A= , CM000671.1:g.117566393A=	GRCh37
NC_000009.10:g.116606214A=	NCBI36
NG_011488.2:g.7016T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374045.5:c.210+1690T= MANE Select	ENSP00000363157.3:n.210+1690T=
ENST00000374045.4:c.210+1690T=	ENSP00000363157.3:n.210+1690T=
NM_005118.3:c.210+1690T=	NP_005109.2:n.210+1690T=
NM_005118.4:c.210+1690T= MANE Select	NP_005109.2:n.210+1690T=