Canonical Allele Identifier: CA403626979

Gene: TNFSF14

Linked Data

• dbSNP Id: rs1461476323
• gnomAD v2: 19-6669896-T-C
• gnomAD v4: 19-6669885-T-C
• MyVariant Identifiers: chr19:g.6669896T>C (hg19) ; chr19:g.6669885T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6669885T>C , CM000681.2:g.6669885T>C	GRCh38
NC_000019.9:g.6669896T>C , CM000681.1:g.6669896T>C	GRCh37
NC_000019.8:g.6620896T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000675206.1:c.185A>G MANE Select	ENSP00000502837.1:p.His62Arg
ENST00000245912.7:c.111+74A>G	ENSP00000245912.3:n.111+74A>G
ENST00000599359.1:c.185A>G	ENSP00000469049.1:p.His62Arg
NM_003807.3:c.185A>G	NP_003798.2:p.His62Arg
NM_172014.2:c.111+74A>G	NP_742011.2:n.111+74A>G
XM_005259670.2:c.111+74A>G	XP_005259727.1:n.111+74A>G
XM_011528398.1:c.185A>G	XP_011526700.1:p.His62Arg
XR_936212.1:n.699A>G
NM_003807.4:c.185A>G	NP_003798.2:p.His62Arg
NM_172014.3:c.111+74A>G	NP_742011.2:n.111+74A>G
XM_017027417.1:c.185A>G	XP_016882906.1:p.His62Arg
XM_017027418.1:c.185A>G	XP_016882907.1:p.His62Arg
XR_001753777.1:n.711A>G
XR_936212.2:n.711A>G
NM_001376887.1:c.185A>G MANE Select	NP_001363816.1:p.His62Arg
NM_003807.5:c.185A>G	NP_003798.2:p.His62Arg