Canonical Allele Identifier: CA728422358

Gene: CCL5

Linked Data

• dbSNP Id: rs1184511495
• gnomAD v3: 17-35880336-A-G
• gnomAD v4: 17-35880336-A-G
• MyVariant Identifiers: chr17:g.35880336A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35880336A>G , CM000679.2:g.35880336A>G	GRCh38
NC_000017.9:g.31231453A>G	NCBI36
NG_015990.1:g.5038T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000603197.6:c.-31T>C	ENSP00000474412.1:n.-31T>C
ENST00000605140.6:c.-31T>C MANE Select	ENSP00000475057.1:n.-31T>C
ENST00000605509.2:c.-17-14T>C	ENSP00000474141.2:n.-17-14T>C
ENST00000651122.1:c.-31T>C	ENSP00000499138.1:n.-31T>C
ENST00000603197.5:c.-31T>C	ENSP00000474412.1:n.-31T>C
ENST00000605140.5:c.-17-14T>C	ENSP00000475057.1:n.-17-14T>C
NM_001278736.1:c.-31T>C	NP_001265665.1:n.-31T>C
NM_002985.2:c.-31T>C	NP_002976.2:n.-31T>C
XR_934696.1:n.197-4046A>G
XR_934697.1:n.200-4046A>G
XR_001752852.1:n.426+262A>G
XR_934696.2:n.91-4046A>G
XR_934697.2:n.91-4046A>G
NM_001278736.2:c.-31T>C	NP_001265665.1:n.-31T>C
NM_002985.3:c.-31T>C MANE Select	NP_002976.2:n.-31T>C