Canonical Allele Identifier: CA1128366610
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1829671216
gnomAD v3: 9-114796287-C-G
gnomAD v4: 9-114796287-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796287C>G , CM000671.2:g.114796287C>G GRCh38
NC_000009.11:g.117558567C>G , CM000671.1:g.117558567C>G GRCh37
NC_000009.10:g.116598388C>G NCBI36
NG_011488.2:g.14842G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2719G>C MANE Select ENSP00000363157.3:n.211-2719G>C
ENST00000374045.4:c.211-2719G>C ENSP00000363157.3:n.211-2719G>C
NM_005118.3:c.211-2719G>C NP_005109.2:n.211-2719G>C
NM_005118.4:c.211-2719G>C MANE Select NP_005109.2:n.211-2719G>C
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