Canonical Allele Identifier: CA505117950

Gene: TNFSF14

Linked Data

• gnomAD v4: 19-6669986-G-A
• MyVariant Identifiers: chr19:g.6669997G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669986G>A , CM000681.2:g.6669986G>A	GRCh38
NC_000019.9:g.6669997G>A , CM000681.1:g.6669997G>A	GRCh37
NC_000019.8:g.6620997G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.84C>T MANE Select	ENSP00000502837.1:p.His28=
ENST00000245912.7:c.84C>T	ENSP00000245912.3:p.His28=
ENST00000599359.1:c.84C>T	ENSP00000469049.1:p.His28=
NM_003807.3:c.84C>T	NP_003798.2:p.His28=
NM_172014.2:c.84C>T	NP_742011.2:p.His28=
XM_005259670.2:c.84C>T	XP_005259727.1:p.His28=
XM_011528398.1:c.84C>T	XP_011526700.1:p.His28=
XR_936212.1:n.598C>T
NM_003807.4:c.84C>T	NP_003798.2:p.His28=
NM_172014.3:c.84C>T	NP_742011.2:p.His28=
XM_017027417.1:c.84C>T	XP_016882906.1:p.His28=
XM_017027418.1:c.84C>T	XP_016882907.1:p.His28=
XR_001753777.1:n.610C>T
XR_936212.2:n.610C>T
NM_001376887.1:c.84C>T MANE Select	NP_001363816.1:p.His28=
NM_003807.5:c.84C>T	NP_003798.2:p.His28=