Canonical Allele Identifier: CA1128366613
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1829671312

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796293G>C , CM000671.2:g.114796293G>C GRCh38
NC_000009.11:g.117558573G>C , CM000671.1:g.117558573G>C GRCh37
NC_000009.10:g.116598394G>C NCBI36
NG_011488.2:g.14836C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2725C>G MANE Select ENSP00000363157.3:n.211-2725C>G
ENST00000374045.4:c.211-2725C>G ENSP00000363157.3:n.211-2725C>G
NM_005118.3:c.211-2725C>G NP_005109.2:n.211-2725C>G
NM_005118.4:c.211-2725C>G MANE Select NP_005109.2:n.211-2725C>G