HGVS | Genome Assembly |
---|---|
NC_000003.12:g.46372935C>T , CM000665.2:g.46372935C>T | GRCh38 |
NC_000003.11:g.46414426C>T , CM000665.1:g.46414426C>T | GRCh37 |
NC_000003.10:g.46389430C>T | NCBI36 |
NG_012637.1:g.7794C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000292303.5:c.33C>T (CCR5) MANE Select | ENSP00000292303.4:p.Asp11= | |
ENST00000292303.4:c.33C>T (CCR5) | ENSP00000292303.4:p.Asp11= | |
ENST00000445772.1:c.33C>T (CCR5) | ENSP00000404881.1:p.Asp11= | |
NM_000579.3:c.33C>T (CCR5) | NP_000570.1:p.Asp11= | |
NM_001100168.1:c.33C>T (CCR5) | NP_001093638.1:p.Asp11= | |
NR_125406.1:n.392-1518G>A (CCR5AS) | ||
NM_000579.4:c.33C>T (CCR5) | NP_000570.1:p.Asp11= | |
NM_001100168.2:c.33C>T (CCR5) | NP_001093638.1:p.Asp11= | |
NM_001394783.1:c.33C>T (CCR5) MANE Select | NP_001381712.1:p.Asp11= |