Canonical Allele Identifier: CA1362081419

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370771C= , CM000665.2:g.46370771C= GRCh38
NC_000003.11:g.46412262C= , CM000665.1:g.46412262C= GRCh37
NC_000003.10:g.46387266C= NCBI36
NG_012637.1:g.5630C=

Transcript Alleles

HGVS Amino-acid Change
NM_000579.3:c.-229C= (CCR5) NP_000570.1:n.-229C=
NM_001100168.1:c.-65-164C= (CCR5) NP_001093638.1:n.-65-164C=
NR_125406.1:n.565+473G= (CCR5AS)
NM_000579.4:c.-229C= (CCR5) NP_000570.1:n.-229C=
NM_001100168.2:c.-65-164C= (CCR5) NP_001093638.1:n.-65-164C=