Canonical Allele Identifier: CA198900154
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1044723758
gnomAD v3: 9-114796317-C-G
gnomAD v4: 9-114796317-C-G
MyVariant Identifiers: chr9:g.117558597C>G (hg19) chr9:g.114796317C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796317C>G , CM000671.2:g.114796317C>G GRCh38
NC_000009.11:g.117558597C>G , CM000671.1:g.117558597C>G GRCh37
NC_000009.10:g.116598418C>G NCBI36
NG_011488.2:g.14812G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2749G>C MANE Select ENSP00000363157.3:n.211-2749G>C
ENST00000374045.4:c.211-2749G>C ENSP00000363157.3:n.211-2749G>C
NM_005118.3:c.211-2749G>C NP_005109.2:n.211-2749G>C
NM_005118.4:c.211-2749G>C MANE Select NP_005109.2:n.211-2749G>C
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