Canonical Allele Identifier: CA198900172
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs111787815
gnomAD v2: 9-117558760-C-A
gnomAD v3: 9-114796480-C-A
gnomAD v4: 9-114796480-C-A
MyVariant Identifiers: chr9:g.117558760C>A (hg19) chr9:g.114796480C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796480C>A , CM000671.2:g.114796480C>A GRCh38
NC_000009.11:g.117558760C>A , CM000671.1:g.117558760C>A GRCh37
NC_000009.10:g.116598581C>A NCBI36
NG_011488.2:g.14649G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2912G>T MANE Select ENSP00000363157.3:n.211-2912G>T
ENST00000374045.4:c.211-2912G>T ENSP00000363157.3:n.211-2912G>T
NM_005118.3:c.211-2912G>T NP_005109.2:n.211-2912G>T
NM_005118.4:c.211-2912G>T MANE Select NP_005109.2:n.211-2912G>T
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