Canonical Allele Identifier: CA2581871376

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370170A>T , CM000665.2:g.46370170A>T GRCh38
NC_000003.11:g.46411661A>T , CM000665.1:g.46411661A>T GRCh37
NC_000003.10:g.46386665A>T NCBI36
NG_012637.1:g.5029A>T

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-329A>T (CCR5) NP_000570.1:n.-329A>T
NM_001100168.1:c.-94A>T (CCR5) NP_001093638.1:n.-94A>T
NR_125406.1:n.565+1074T>A (CCR5AS)
NM_000579.4:c.-329A>T (CCR5) NP_000570.1:n.-329A>T
NM_001100168.2:c.-94A>T (CCR5) NP_001093638.1:n.-94A>T