Canonical Allele Identifier: CA198900166
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs893267934
gnomAD v3: 9-114796441-T-C
gnomAD v4: 9-114796441-T-C
MyVariant Identifiers: chr9:g.117558721T>C (hg19) chr9:g.114796441T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796441T>C , CM000671.2:g.114796441T>C GRCh38
NC_000009.11:g.117558721T>C , CM000671.1:g.117558721T>C GRCh37
NC_000009.10:g.116598542T>C NCBI36
NG_011488.2:g.14688A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2873A>G MANE Select ENSP00000363157.3:n.211-2873A>G
ENST00000374045.4:c.211-2873A>G ENSP00000363157.3:n.211-2873A>G
NM_005118.3:c.211-2873A>G NP_005109.2:n.211-2873A>G
NM_005118.4:c.211-2873A>G MANE Select NP_005109.2:n.211-2873A>G
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