Canonical Allele Identifier: CA2720482329
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1325426911
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785418C>T , CM000671.2:g.114785418C>T GRCh38
NC_000009.11:g.117547698C>T , CM000671.1:g.117547698C>T GRCh37
NC_000009.10:g.116587519C>T NCBI36
NG_011488.2:g.25711G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5034G>A MANE Select ENSP00000363157.3:n.*5034G>A
ENST00000374045.4:c.*5034G>A ENSP00000363157.3:n.*5034G>A
NM_001204344.1:c.5613G>A NP_001191273.1:n.5613G>A
NM_005118.3:c.*5034G>A NP_005109.2:n.*5034G>A
NM_005118.4:c.*5034G>A MANE Select NP_005109.2:n.*5034G>A
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