Canonical Allele Identifier: CA1128363698
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1829486359
gnomAD v3: 9-114785540-C-A
gnomAD v4: 9-114785540-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785540C>A , CM000671.2:g.114785540C>A GRCh38
NC_000009.11:g.117547820C>A , CM000671.1:g.117547820C>A GRCh37
NC_000009.10:g.116587641C>A NCBI36
NG_011488.2:g.25589G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4912G>T MANE Select ENSP00000363157.3:n.*4912G>T
ENST00000374045.4:c.*4912G>T ENSP00000363157.3:n.*4912G>T
NM_001204344.1:c.5491G>T NP_001191273.1:n.5491G>T
NM_005118.3:c.*4912G>T NP_005109.2:n.*4912G>T
NM_005118.4:c.*4912G>T MANE Select NP_005109.2:n.*4912G>T
Search 100 bp 5'
Search 100 bp 3'