Canonical Allele Identifier: CA2691385628
Gene: TNFSF15 HGNC NCBI

Linked Data

gnomAD v4: 9-114785483-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785483C>G , CM000671.2:g.114785483C>G GRCh38
NC_000009.11:g.117547763C>G , CM000671.1:g.117547763C>G GRCh37
NC_000009.10:g.116587584C>G NCBI36
NG_011488.2:g.25646G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4969G>C MANE Select ENSP00000363157.3:n.*4969G>C
ENST00000374045.4:c.*4969G>C ENSP00000363157.3:n.*4969G>C
NM_001204344.1:c.5548G>C NP_001191273.1:n.5548G>C
NM_005118.3:c.*4969G>C NP_005109.2:n.*4969G>C
NM_005118.4:c.*4969G>C MANE Select NP_005109.2:n.*4969G>C
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