Canonical Allele Identifier: CA198901029
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs993836858
gnomAD v2: 9-117566385-C-T
gnomAD v3: 9-114804105-C-T
gnomAD v4: 9-114804105-C-T
MyVariant Identifiers: chr9:g.117566385C>T (hg19) chr9:g.114804105C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114804105C>T , CM000671.2:g.114804105C>T GRCh38
NC_000009.11:g.117566385C>T , CM000671.1:g.117566385C>T GRCh37
NC_000009.10:g.116606206C>T NCBI36
NG_011488.2:g.7024G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.210+1698G>A MANE Select ENSP00000363157.3:n.210+1698G>A
ENST00000374045.4:c.210+1698G>A ENSP00000363157.3:n.210+1698G>A
NM_005118.3:c.210+1698G>A NP_005109.2:n.210+1698G>A
NM_005118.4:c.210+1698G>A MANE Select NP_005109.2:n.210+1698G>A
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