Canonical Allele Identifier: CA290054760
Gene: CCL5 HGNC NCBI

Linked Data

dbSNP Id: rs945106333
MyVariant Identifiers: chr17:g.35880609T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880609T>A , CM000679.2:g.35880609T>A GRCh38
NC_000017.9:g.31231726T>A NCBI36
NG_015990.1:g.4765A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000605509.2:c.-18+120A>T ENSP00000474141.2:n.-18+120A>T
ENST00000605140.5:c.-18+120A>T ENSP00000475057.1:n.-18+120A>T
XR_934696.1:n.197-3773T>A
XR_934697.1:n.200-3773T>A
XR_001752852.1:n.426+535T>A
XR_934696.2:n.91-3773T>A
XR_934697.2:n.91-3773T>A