Canonical Allele Identifier: CA520787188

Gene: TNFRSF9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7929506C>A , CM000663.2:g.7929506C>A	GRCh38
NC_000001.10:g.7989566C>A , CM000663.1:g.7989566C>A	GRCh37
NC_000001.9:g.7912153C>A	NCBI36
NG_052834.1:g.18660G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377507.8:c.679+3656G>T MANE Select	ENSP00000366729.3:n.679+3656G>T
ENST00000377507.7:c.679+3656G>T	ENSP00000366729.3:n.679+3656G>T
ENST00000474475.1:c.223+3656G>T	ENSP00000465272.1:n.223+3656G>T
ENST00000615230.4:c.679+3656G>T	ENSP00000478699.1:n.679+3656G>T
NM_001561.5:c.679+3656G>T	NP_001552.2:n.679+3656G>T
XM_006710618.2:c.679+3656G>T	XP_006710681.1:n.679+3656G>T
XM_011541386.1:c.679+3656G>T	XP_011539688.1:n.679+3656G>T
XM_006710618.3:c.679+3656G>T	XP_006710681.1:n.679+3656G>T
XM_011541386.2:c.679+3656G>T	XP_011539688.1:n.679+3656G>T
NM_001561.6:c.679+3656G>T MANE Select	NP_001552.2:n.679+3656G>T