Canonical Allele Identifier: CA1362081170

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370197G= , CM000665.2:g.46370197G= GRCh38
NC_000003.11:g.46411688G= , CM000665.1:g.46411688G= GRCh37
NC_000003.10:g.46386692G= NCBI36
NG_012637.1:g.5056G=

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-302G= (CCR5) NP_000570.1:n.-302G=
NM_001100168.1:c.-67G= (CCR5) NP_001093638.1:n.-67G=
NR_125406.1:n.565+1047C= (CCR5AS)
NM_000579.4:c.-302G= (CCR5) NP_000570.1:n.-302G=
NM_001100168.2:c.-67G= (CCR5) NP_001093638.1:n.-67G=