Canonical Allele Identifier: CA290054620

Gene: CCL5

Linked Data

• dbSNP Id: rs372088244
• gnomAD v3: 17-35880321-G-A
• gnomAD v4: 17-35880321-G-A
• MyVariant Identifiers: chr17:g.35880321G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35880321G>A , CM000679.2:g.35880321G>A	GRCh38
NC_000017.9:g.31231438G>A	NCBI36
NG_015990.1:g.5053C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000603197.6:c.-16C>T	ENSP00000474412.1:n.-16C>T
ENST00000605140.6:c.-16C>T MANE Select	ENSP00000475057.1:n.-16C>T
ENST00000605509.2:c.-16C>T	ENSP00000474141.2:n.-16C>T
ENST00000651122.1:c.-16C>T	ENSP00000499138.1:n.-16C>T
ENST00000603197.5:c.-16C>T	ENSP00000474412.1:n.-16C>T
ENST00000605140.5:c.-16C>T	ENSP00000475057.1:n.-16C>T
NM_001278736.1:c.-16C>T	NP_001265665.1:n.-16C>T
NM_002985.2:c.-16C>T	NP_002976.2:n.-16C>T
XR_934696.1:n.197-4061G>A
XR_934697.1:n.200-4061G>A
XR_001752852.1:n.426+247G>A
XR_934696.2:n.91-4061G>A
XR_934697.2:n.91-4061G>A
NM_001278736.2:c.-16C>T	NP_001265665.1:n.-16C>T
NM_002985.3:c.-16C>T MANE Select	NP_002976.2:n.-16C>T