Canonical Allele Identifier: CA1874001257
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1564345852
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796321A>C , CM000671.2:g.114796321A>C GRCh38
NC_000009.11:g.117558601A>C , CM000671.1:g.117558601A>C GRCh37
NC_000009.10:g.116598422A>C NCBI36
NG_011488.2:g.14808T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2753T>G MANE Select ENSP00000363157.3:n.211-2753T>G
ENST00000374045.4:c.211-2753T>G ENSP00000363157.3:n.211-2753T>G
NM_005118.3:c.211-2753T>G NP_005109.2:n.211-2753T>G
NM_005118.4:c.211-2753T>G MANE Select NP_005109.2:n.211-2753T>G
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