Canonical Allele Identifier: CA2354659
Gene: CCR5 HGNC NCBI

Linked Data

dbSNP Id: rs55639502

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373379G>C , CM000665.2:g.46373379G>C GRCh38
NC_000003.11:g.46414870G>C , CM000665.1:g.46414870G>C GRCh37
NC_000003.10:g.46389874G>C NCBI36
NG_012637.1:g.8238G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.4:c.477G>C ENSP00000292303.4:p.Ala159=
ENST00000445772.1:c.477G>C ENSP00000404881.1:p.Ala159=
NM_000579.3:c.477G>C NP_000570.1:p.Ala159=
NM_001100168.1:c.477G>C NP_001093638.1:p.Ala159=
NM_000579.4:c.477G>C NP_000570.1:p.Ala159=
NM_001100168.2:c.477G>C NP_001093638.1:p.Ala159=