Canonical Allele Identifier: CA728422610
Gene: CCL5 HGNC NCBI

Linked Data

dbSNP Id: rs1410437565
MyVariant Identifiers: chr17:g.35880699A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880699A>G , CM000679.2:g.35880699A>G GRCh38
NC_000017.9:g.31231816A>G NCBI36
NG_015990.1:g.4675T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000605509.2:c.-18+30T>C ENSP00000474141.2:n.-18+30T>C
ENST00000605140.5:c.-18+30T>C ENSP00000475057.1:n.-18+30T>C
XR_934696.1:n.197-3683A>G
XR_934697.1:n.200-3683A>G
XR_001752852.1:n.426+625A>G
XR_934696.2:n.91-3683A>G
XR_934697.2:n.91-3683A>G