Canonical Allele Identifier: CA1128367442
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1829786118

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114804200T>A , CM000671.2:g.114804200T>A GRCh38
NC_000009.11:g.117566480T>A , CM000671.1:g.117566480T>A GRCh37
NC_000009.10:g.116606301T>A NCBI36
NG_011488.2:g.6929A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.210+1603A>T MANE Select ENSP00000363157.3:n.210+1603A>T
ENST00000374045.4:c.210+1603A>T ENSP00000363157.3:n.210+1603A>T
NM_005118.3:c.210+1603A>T NP_005109.2:n.210+1603A>T
NM_005118.4:c.210+1603A>T MANE Select NP_005109.2:n.210+1603A>T