Canonical Allele Identifier: CA1362081249

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370392G= , CM000665.2:g.46370392G= GRCh38
NC_000003.11:g.46411883G= , CM000665.1:g.46411883G= GRCh37
NC_000003.10:g.46386887G= NCBI36
NG_012637.1:g.5251G=

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+194G= (CCR5) NP_000570.1:n.-301+194G=
NM_001100168.1:c.-66+194G= (CCR5) NP_001093638.1:n.-66+194G=
NR_125406.1:n.565+852C= (CCR5AS)
NM_000579.4:c.-301+194G= (CCR5) NP_000570.1:n.-301+194G=
NM_001100168.2:c.-66+194G= (CCR5) NP_001093638.1:n.-66+194G=