Canonical Allele Identifier: CA2257705485
Gene: CCL5 HGNC NCBI

Linked Data

dbSNP Id: rs3817655

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35872637A>G , CM000679.2:g.35872637A>G GRCh38
NC_000017.9:g.31223754A>G NCBI36
NG_015990.1:g.12737T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000603197.6:c.189-173T>C ENSP00000474412.1:n.189-173T>C
ENST00000605140.6:c.189-173T>C MANE Select ENSP00000475057.1:n.189-173T>C
ENST00000605509.2:c.189-173T>C ENSP00000474141.2:n.189-173T>C
ENST00000651122.1:c.271-173T>C ENSP00000499138.1:n.271-173T>C
ENST00000603197.5:c.189-173T>C ENSP00000474412.1:n.189-173T>C
ENST00000605140.5:c.189-173T>C ENSP00000475057.1:n.189-173T>C
ENST00000605509.1:c.257-173T>C
NM_001278736.1:c.271-173T>C NP_001265665.1:n.271-173T>C
NM_002985.2:c.189-173T>C NP_002976.2:n.189-173T>C
XR_934696.1:n.196+3519A>G
XR_934697.1:n.199+3519A>G
XR_934696.2:n.90+3519A>G
XR_934697.2:n.90+3519A>G
NM_001278736.2:c.271-173T>C NP_001265665.1:n.271-173T>C
NM_002985.3:c.189-173T>C MANE Select NP_002976.2:n.189-173T>C