Canonical Allele Identifier: CA1362081251

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370395T= , CM000665.2:g.46370395T= GRCh38
NC_000003.11:g.46411886T= , CM000665.1:g.46411886T= GRCh37
NC_000003.10:g.46386890T= NCBI36
NG_012637.1:g.5254T=

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+197T= (CCR5) NP_000570.1:n.-301+197T=
NM_001100168.1:c.-66+197T= (CCR5) NP_001093638.1:n.-66+197T=
NR_125406.1:n.565+849A= (CCR5AS)
NM_000579.4:c.-301+197T= (CCR5) NP_000570.1:n.-301+197T=
NM_001100168.2:c.-66+197T= (CCR5) NP_001093638.1:n.-66+197T=