Canonical Allele Identifier: CA1362081246

Linked Data

dbSNP Id: rs1369480639

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370384G>A , CM000665.2:g.46370384G>A GRCh38
NC_000003.11:g.46411875G>A , CM000665.1:g.46411875G>A GRCh37
NC_000003.10:g.46386879G>A NCBI36
NG_012637.1:g.5243G>A

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+186G>A (CCR5) NP_000570.1:n.-301+186G>A
NM_001100168.1:c.-66+186G>A (CCR5) NP_001093638.1:n.-66+186G>A
NR_125406.1:n.565+860C>T (CCR5AS)
NM_000579.4:c.-301+186G>A (CCR5) NP_000570.1:n.-301+186G>A
NM_001100168.2:c.-66+186G>A (CCR5) NP_001093638.1:n.-66+186G>A