Canonical Allele Identifier: CA1362082325

Linked Data

dbSNP Id: rs1701682307
gnomAD v4: 3-46372891-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46372891G>A , CM000665.2:g.46372891G>A GRCh38
NC_000003.11:g.46414382G>A , CM000665.1:g.46414382G>A GRCh37
NC_000003.10:g.46389386G>A NCBI36
NG_012637.1:g.7750G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.-11-1G>A (CCR5) MANE Select ENSP00000292303.4:n.-11-1G>A
ENST00000292303.4:c.-11-1G>A (CCR5) ENSP00000292303.4:n.-11-1G>A
ENST00000445772.1:c.-12G>A (CCR5) ENSP00000404881.1:n.-12G>A
NM_000579.3:c.-11-1G>A (CCR5) NP_000570.1:n.-11-1G>A
NM_001100168.1:c.-11-1G>A (CCR5) NP_001093638.1:n.-11-1G>A
NR_125406.1:n.392-1474C>T (CCR5AS)
NM_000579.4:c.-11-1G>A (CCR5) NP_000570.1:n.-11-1G>A
NM_001100168.2:c.-11-1G>A (CCR5) NP_001093638.1:n.-11-1G>A
NM_001394783.1:c.-11-1G>A (CCR5) MANE Select NP_001381712.1:n.-11-1G>A