Canonical Allele Identifier: CA2691385631
Gene: TNFSF15 HGNC NCBI

Linked Data

gnomAD v4: 9-114785493-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785493A>T , CM000671.2:g.114785493A>T GRCh38
NC_000009.11:g.117547773A>T , CM000671.1:g.117547773A>T GRCh37
NC_000009.10:g.116587594A>T NCBI36
NG_011488.2:g.25636T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.*4959T>A MANE Select ENSP00000363157.3:n.*4959T>A
ENST00000374045.4:c.*4959T>A ENSP00000363157.3:n.*4959T>A
NM_001204344.1:c.5538T>A NP_001191273.1:n.5538T>A
NM_005118.3:c.*4959T>A NP_005109.2:n.*4959T>A
NM_005118.4:c.*4959T>A MANE Select NP_005109.2:n.*4959T>A
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