Canonical Allele Identifier: CA728422440
Gene: CCL5 HGNC NCBI

Linked Data

dbSNP Id: rs1463693152
MyVariant Identifiers: chr17:g.35880414T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880414T>C , CM000679.2:g.35880414T>C GRCh38
NC_000017.9:g.31231531T>C NCBI36
NG_015990.1:g.4960A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000603197.6:c.-109A>G ENSP00000474412.1:n.-109A>G
ENST00000605509.2:c.-17-92A>G ENSP00000474141.2:n.-17-92A>G
ENST00000603197.5:c.-109A>G ENSP00000474412.1:n.-109A>G
ENST00000605140.5:c.-17-92A>G ENSP00000475057.1:n.-17-92A>G
XR_934696.1:n.197-3968T>C
XR_934697.1:n.200-3968T>C
XR_001752852.1:n.426+340T>C
XR_934696.2:n.91-3968T>C
XR_934697.2:n.91-3968T>C