Canonical Allele Identifier: CA1362081231

Linked Data

dbSNP Id: rs1701645047

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46370346G>T , CM000665.2:g.46370346G>T GRCh38
NC_000003.11:g.46411837G>T , CM000665.1:g.46411837G>T GRCh37
NC_000003.10:g.46386841G>T NCBI36
NG_012637.1:g.5205G>T

Transcript Alleles

HGVS Amino-acid change
NM_000579.3:c.-301+148G>T (CCR5) NP_000570.1:n.-301+148G>T
NM_001100168.1:c.-66+148G>T (CCR5) NP_001093638.1:n.-66+148G>T
NR_125406.1:n.565+898C>A (CCR5AS)
NM_000579.4:c.-301+148G>T (CCR5) NP_000570.1:n.-301+148G>T
NM_001100168.2:c.-66+148G>T (CCR5) NP_001093638.1:n.-66+148G>T