Canonical Allele Identifier: CA9128115

Gene: TNFSF14

Linked Data

• dbSNP Id: rs769318404
• ExAC: 19:6669891 G / A
• gnomAD v2: 19-6669891-G-A
• gnomAD v4: 19-6669880-G-A
• MyVariant Identifiers: chr19:g.6669891G>A (hg19) ; chr19:g.6669880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669880G>A , CM000681.2:g.6669880G>A	GRCh38
NC_000019.9:g.6669891G>A , CM000681.1:g.6669891G>A	GRCh37
NC_000019.8:g.6620891G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.190C>T MANE Select	ENSP00000502837.1:p.Arg64Cys
ENST00000245912.7:c.111+79C>T	ENSP00000245912.3:n.111+79C>T
ENST00000599359.1:c.190C>T	ENSP00000469049.1:p.Arg64Cys
NM_003807.3:c.190C>T	NP_003798.2:p.Arg64Cys
NM_172014.2:c.111+79C>T	NP_742011.2:n.111+79C>T
XM_005259670.2:c.111+79C>T	XP_005259727.1:n.111+79C>T
XM_011528398.1:c.190C>T	XP_011526700.1:p.Arg64Cys
XR_936212.1:n.704C>T
NM_003807.4:c.190C>T	NP_003798.2:p.Arg64Cys
NM_172014.3:c.111+79C>T	NP_742011.2:n.111+79C>T
XM_017027417.1:c.190C>T	XP_016882906.1:p.Arg64Cys
XM_017027418.1:c.190C>T	XP_016882907.1:p.Arg64Cys
XR_001753777.1:n.716C>T
XR_936212.2:n.716C>T
NM_001376887.1:c.190C>T MANE Select	NP_001363816.1:p.Arg64Cys
NM_003807.5:c.190C>T	NP_003798.2:p.Arg64Cys