Canonical Allele Identifier: CA2354659

Linked Data

dbSNP Id: rs55639502
gnomAD v2: 3-46414870-G-C
gnomAD v3: 3-46373379-G-C
gnomAD v4: 3-46373379-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373379G>C , CM000665.2:g.46373379G>C GRCh38
NC_000003.11:g.46414870G>C , CM000665.1:g.46414870G>C GRCh37
NC_000003.10:g.46389874G>C NCBI36
NG_012637.1:g.8238G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.5:c.477G>C (CCR5) MANE Select ENSP00000292303.4:p.Ala159=
ENST00000292303.4:c.477G>C (CCR5) ENSP00000292303.4:p.Ala159=
ENST00000445772.1:c.477G>C (CCR5) ENSP00000404881.1:p.Ala159=
NM_000579.3:c.477G>C (CCR5) NP_000570.1:p.Ala159=
NM_001100168.1:c.477G>C (CCR5) NP_001093638.1:p.Ala159=
NR_125406.1:n.392-1962C>G (CCR5AS)
NM_000579.4:c.477G>C (CCR5) NP_000570.1:p.Ala159=
NM_001100168.2:c.477G>C (CCR5) NP_001093638.1:p.Ala159=
NM_001394783.1:c.477G>C (CCR5) MANE Select NP_001381712.1:p.Ala159=