Canonical Allele Identifier: CA9128139

Gene: TNFSF14

Linked Data

• dbSNP Id: rs201980574
• ExAC: 19:6670017 T / C
• gnomAD v2: 19-6670017-T-C
• gnomAD v3: 19-6670006-T-C
• gnomAD v4: 19-6670006-T-C
• MyVariant Identifiers: chr19:g.6670017T>C (hg19) ; chr19:g.6670006T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6670006T>C , CM000681.2:g.6670006T>C	GRCh38
NC_000019.9:g.6670017T>C , CM000681.1:g.6670017T>C	GRCh37
NC_000019.8:g.6621017T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675206.1:c.64A>G MANE Select	ENSP00000502837.1:p.Thr22Ala
ENST00000245912.7:c.64A>G	ENSP00000245912.3:p.Thr22Ala
ENST00000599359.1:c.64A>G	ENSP00000469049.1:p.Thr22Ala
NM_003807.3:c.64A>G	NP_003798.2:p.Thr22Ala
NM_172014.2:c.64A>G	NP_742011.2:p.Thr22Ala
XM_005259670.2:c.64A>G	XP_005259727.1:p.Thr22Ala
XM_011528398.1:c.64A>G	XP_011526700.1:p.Thr22Ala
XR_936212.1:n.578A>G
NM_003807.4:c.64A>G	NP_003798.2:p.Thr22Ala
NM_172014.3:c.64A>G	NP_742011.2:p.Thr22Ala
XM_017027417.1:c.64A>G	XP_016882906.1:p.Thr22Ala
XM_017027418.1:c.64A>G	XP_016882907.1:p.Thr22Ala
XR_001753777.1:n.590A>G
XR_936212.2:n.590A>G
NM_001376887.1:c.64A>G MANE Select	NP_001363816.1:p.Thr22Ala
NM_003807.5:c.64A>G	NP_003798.2:p.Thr22Ala