Linked Data
dbSNP Id:
rs371598347
gnomAD v2:
3-46415040-G-C
gnomAD v3:
3-46373549-G-C
gnomAD v4:
3-46373549-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46373549G>C , CM000665.2:g.46373549G>C | GRCh38 |
| NC_000003.11:g.46415040G>C , CM000665.1:g.46415040G>C | GRCh37 |
| NC_000003.10:g.46390044G>C | NCBI36 |
| NG_012637.1:g.8408G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292303.5:c.647G>C (CCR5) MANE Select | ENSP00000292303.4:p.Gly216Ala | |
| ENST00000292303.4:c.647G>C (CCR5) | ENSP00000292303.4:p.Gly216Ala | |
| ENST00000445772.1:c.647G>C (CCR5) | ENSP00000404881.1:p.Gly216Ala | |
| NM_000579.3:c.647G>C (CCR5) | NP_000570.1:p.Gly216Ala | |
| NM_001100168.1:c.647G>C (CCR5) | NP_001093638.1:p.Gly216Ala | |
| NR_125406.1:n.392-2132C>G (CCR5AS) | ||
| NM_000579.4:c.647G>C (CCR5) | NP_000570.1:p.Gly216Ala | |
| NM_001100168.2:c.647G>C (CCR5) | NP_001093638.1:p.Gly216Ala | |
| NM_001394783.1:c.647G>C (CCR5) MANE Select | NP_001381712.1:p.Gly216Ala |