Canonical Allele Identifier: CA1362081238

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370367C= , CM000665.2:g.46370367C= GRCh38
NC_000003.11:g.46411858C= , CM000665.1:g.46411858C= GRCh37
NC_000003.10:g.46386862C= NCBI36
NG_012637.1:g.5226C=

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+169C= (CCR5) NP_000570.1:n.-301+169C=
NM_001100168.1:c.-66+169C= (CCR5) NP_001093638.1:n.-66+169C=
NR_125406.1:n.565+877G= (CCR5AS)
NM_000579.4:c.-301+169C= (CCR5) NP_000570.1:n.-301+169C=
NM_001100168.2:c.-66+169C= (CCR5) NP_001093638.1:n.-66+169C=