Canonical Allele Identifier: CA1128363682
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1157644574
gnomAD v3: 9-114785451-A-C
gnomAD v4: 9-114785451-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785451A>C , CM000671.2:g.114785451A>C GRCh38
NC_000009.11:g.117547731A>C , CM000671.1:g.117547731A>C GRCh37
NC_000009.10:g.116587552A>C NCBI36
NG_011488.2:g.25678T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5001T>G MANE Select ENSP00000363157.3:n.*5001T>G
ENST00000374045.4:c.*5001T>G ENSP00000363157.3:n.*5001T>G
NM_001204344.1:c.5580T>G NP_001191273.1:n.5580T>G
NM_005118.3:c.*5001T>G NP_005109.2:n.*5001T>G
NM_005118.4:c.*5001T>G MANE Select NP_005109.2:n.*5001T>G
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