Canonical Allele Identifier: CA2691385645
Gene: TNFSF15 HGNC NCBI

Linked Data

gnomAD v4: 9-114785548-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785548G>T , CM000671.2:g.114785548G>T GRCh38
NC_000009.11:g.117547828G>T , CM000671.1:g.117547828G>T GRCh37
NC_000009.10:g.116587649G>T NCBI36
NG_011488.2:g.25581C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4904C>A MANE Select ENSP00000363157.3:n.*4904C>A
ENST00000374045.4:c.*4904C>A ENSP00000363157.3:n.*4904C>A
NM_001204344.1:c.5483C>A NP_001191273.1:n.5483C>A
NM_005118.3:c.*4904C>A NP_005109.2:n.*4904C>A
NM_005118.4:c.*4904C>A MANE Select NP_005109.2:n.*4904C>A
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