Canonical Allele Identifier: CA2354657
Gene: CCR5 HGNC NCBI

Linked Data

dbSNP Id: rs746300015

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373378C>A , CM000665.2:g.46373378C>A GRCh38
NC_000003.11:g.46414869C>A , CM000665.1:g.46414869C>A GRCh37
NC_000003.10:g.46389873C>A NCBI36
NG_012637.1:g.8237C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.4:c.476C>A ENSP00000292303.4:p.Ala159Glu
ENST00000445772.1:c.476C>A ENSP00000404881.1:p.Ala159Glu
NM_000579.3:c.476C>A NP_000570.1:p.Ala159Glu
NM_001100168.1:c.476C>A NP_001093638.1:p.Ala159Glu
NR_125406.1:n.392-1961G>T
NM_000579.4:c.476C>A NP_000570.1:p.Ala159Glu
NM_001100168.2:c.476C>A NP_001093638.1:p.Ala159Glu