Canonical Allele Identifier: CA1362081154

Genomic Alleles

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

Transcript Alleles

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