Canonical Allele Identifier: CA858969397
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1216098267
MyVariant Identifiers: chr9:g.117547654G>A (hg19) chr9:g.114785374G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785374G>A , CM000671.2:g.114785374G>A GRCh38
NC_000009.11:g.117547654G>A , CM000671.1:g.117547654G>A GRCh37
NC_000009.10:g.116587475G>A NCBI36
NG_011488.2:g.25755C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5078C>T MANE Select ENSP00000363157.3:n.*5078C>T
ENST00000374045.4:c.*5078C>T ENSP00000363157.3:n.*5078C>T
NM_001204344.1:c.5657C>T NP_001191273.1:n.5657C>T
NM_005118.3:c.*5078C>T NP_005109.2:n.*5078C>T
NM_005118.4:c.*5078C>T MANE Select NP_005109.2:n.*5078C>T
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