Canonical Allele Identifier: CA1128366623
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1829671530

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796320G>C , CM000671.2:g.114796320G>C GRCh38
NC_000009.11:g.117558600G>C , CM000671.1:g.117558600G>C GRCh37
NC_000009.10:g.116598421G>C NCBI36
NG_011488.2:g.14809C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.211-2752C>G MANE Select ENSP00000363157.3:n.211-2752C>G
ENST00000374045.4:c.211-2752C>G ENSP00000363157.3:n.211-2752C>G
NM_005118.3:c.211-2752C>G NP_005109.2:n.211-2752C>G
NM_005118.4:c.211-2752C>G MANE Select NP_005109.2:n.211-2752C>G