Canonical Allele Identifier: CA1128366601
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1829670769

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796226C>A , CM000671.2:g.114796226C>A GRCh38
NC_000009.11:g.117558506C>A , CM000671.1:g.117558506C>A GRCh37
NC_000009.10:g.116598327C>A NCBI36
NG_011488.2:g.14903G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2658G>T MANE Select ENSP00000363157.3:n.211-2658G>T
ENST00000374045.4:c.211-2658G>T ENSP00000363157.3:n.211-2658G>T
NM_005118.3:c.211-2658G>T NP_005109.2:n.211-2658G>T
NM_005118.4:c.211-2658G>T MANE Select NP_005109.2:n.211-2658G>T