Linked Data
dbSNP Id:
rs747625967
ExAC:
3:46415039 G / A
gnomAD v2:
3-46415039-G-A
gnomAD v4:
3-46373548-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46373548G>A , CM000665.2:g.46373548G>A | GRCh38 |
| NC_000003.11:g.46415039G>A , CM000665.1:g.46415039G>A | GRCh37 |
| NC_000003.10:g.46390043G>A | NCBI36 |
| NG_012637.1:g.8407G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292303.5:c.646G>A (CCR5) MANE Select | ENSP00000292303.4:p.Gly216Arg | |
| ENST00000292303.4:c.646G>A (CCR5) | ENSP00000292303.4:p.Gly216Arg | |
| ENST00000445772.1:c.646G>A (CCR5) | ENSP00000404881.1:p.Gly216Arg | |
| NM_000579.3:c.646G>A (CCR5) | NP_000570.1:p.Gly216Arg | |
| NM_001100168.1:c.646G>A (CCR5) | NP_001093638.1:p.Gly216Arg | |
| NR_125406.1:n.392-2131C>T (CCR5AS) | ||
| NM_000579.4:c.646G>A (CCR5) | NP_000570.1:p.Gly216Arg | |
| NM_001100168.2:c.646G>A (CCR5) | NP_001093638.1:p.Gly216Arg | |
| NM_001394783.1:c.646G>A (CCR5) MANE Select | NP_001381712.1:p.Gly216Arg |