Linked Data
gnomAD v4:
3-46373358-T-C
COSMIC:
COSM1559678
MyVariant Identifiers:
chr3:g.46414849T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46373358T>C , CM000665.2:g.46373358T>C | GRCh38 |
| NC_000003.11:g.46414849T>C , CM000665.1:g.46414849T>C | GRCh37 |
| NC_000003.10:g.46389853T>C | NCBI36 |
| NG_012637.1:g.8217T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000292303.5:c.456T>C (CCR5) MANE Select | ENSP00000292303.4:p.Thr152= | |
| ENST00000292303.4:c.456T>C (CCR5) | ENSP00000292303.4:p.Thr152= | |
| ENST00000445772.1:c.456T>C (CCR5) | ENSP00000404881.1:p.Thr152= | |
| NM_000579.3:c.456T>C (CCR5) | NP_000570.1:p.Thr152= | |
| NM_001100168.1:c.456T>C (CCR5) | NP_001093638.1:p.Thr152= | |
| NR_125406.1:n.392-1941A>G (CCR5AS) | ||
| NM_000579.4:c.456T>C (CCR5) | NP_000570.1:p.Thr152= | |
| NM_001100168.2:c.456T>C (CCR5) | NP_001093638.1:p.Thr152= | |
| NM_001394783.1:c.456T>C (CCR5) MANE Select | NP_001381712.1:p.Thr152= |