Canonical Allele Identifier: CA728422551
Gene: CCL5 HGNC NCBI

Linked Data

dbSNP Id: rs1431152955
MyVariant Identifiers: chr17:g.35880615del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880615del , CM000679.2:g.35880615del GRCh38
NC_000017.9:g.31231732del NCBI36
NG_015990.1:g.4759del

Transcript Alleles

HGVS Amino-acid Change
ENST00000605509.2:c.-18+114del ENSP00000474141.2:n.-18+114del
ENST00000605140.5:c.-18+114del ENSP00000475057.1:n.-18+114del
XR_934696.1:n.197-3767del
XR_934697.1:n.200-3767del
XR_001752852.1:n.426+541del
XR_934696.2:n.91-3767del
XR_934697.2:n.91-3767del