Canonical Allele Identifier: CA1362081167

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370190T= , CM000665.2:g.46370190T= GRCh38
NC_000003.11:g.46411681T= , CM000665.1:g.46411681T= GRCh37
NC_000003.10:g.46386685T= NCBI36
NG_012637.1:g.5049T=

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-309T= (CCR5) NP_000570.1:n.-309T=
NM_001100168.1:c.-74T= (CCR5) NP_001093638.1:n.-74T=
NR_125406.1:n.565+1054A= (CCR5AS)
NM_000579.4:c.-309T= (CCR5) NP_000570.1:n.-309T=
NM_001100168.2:c.-74T= (CCR5) NP_001093638.1:n.-74T=