Canonical Allele Identifier: CA73681761

Linked Data

dbSNP Id: rs1030899090

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370249A>G , CM000665.2:g.46370249A>G GRCh38
NC_000003.11:g.46411740A>G , CM000665.1:g.46411740A>G GRCh37
NC_000003.10:g.46386744A>G NCBI36
NG_012637.1:g.5108A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000579.3:c.-301+51A>G (CCR5) NP_000570.1:n.-301+51A>G
NM_001100168.1:c.-66+51A>G (CCR5) NP_001093638.1:n.-66+51A>G
NR_125406.1:n.565+995T>C (CCR5AS)
NM_000579.4:c.-301+51A>G (CCR5) NP_000570.1:n.-301+51A>G
NM_001100168.2:c.-66+51A>G (CCR5) NP_001093638.1:n.-66+51A>G