Canonical Allele Identifier: CA352469101

Linked Data

dbSNP Id: rs1701685087

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46372969A>G , CM000665.2:g.46372969A>G GRCh38
NC_000003.11:g.46414460A>G , CM000665.1:g.46414460A>G GRCh37
NC_000003.10:g.46389464A>G NCBI36
NG_012637.1:g.7828A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.67A>G (CCR5) MANE Select ENSP00000292303.4:p.Ile23Val
ENST00000292303.4:c.67A>G (CCR5) ENSP00000292303.4:p.Ile23Val
ENST00000445772.1:c.67A>G (CCR5) ENSP00000404881.1:p.Ile23Val
NM_000579.3:c.67A>G (CCR5) NP_000570.1:p.Ile23Val
NM_001100168.1:c.67A>G (CCR5) NP_001093638.1:p.Ile23Val
NR_125406.1:n.392-1552T>C (CCR5AS)
NM_000579.4:c.67A>G (CCR5) NP_000570.1:p.Ile23Val
NM_001100168.2:c.67A>G (CCR5) NP_001093638.1:p.Ile23Val
NM_001394783.1:c.67A>G (CCR5) MANE Select NP_001381712.1:p.Ile23Val