HGVS | Genome Assembly |
---|---|
NC_000003.12:g.46372909T>C , CM000665.2:g.46372909T>C | GRCh38 |
NC_000003.11:g.46414400T>C , CM000665.1:g.46414400T>C | GRCh37 |
NC_000003.10:g.46389404T>C | NCBI36 |
NG_012637.1:g.7768T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000292303.5:c.7T>C (CCR5) MANE Select | ENSP00000292303.4:p.Tyr3His | |
ENST00000292303.4:c.7T>C (CCR5) | ENSP00000292303.4:p.Tyr3His | |
ENST00000445772.1:c.7T>C (CCR5) | ENSP00000404881.1:p.Tyr3His | |
NM_000579.3:c.7T>C (CCR5) | NP_000570.1:p.Tyr3His | |
NM_001100168.1:c.7T>C (CCR5) | NP_001093638.1:p.Tyr3His | |
NR_125406.1:n.392-1492A>G (CCR5AS) | ||
NM_000579.4:c.7T>C (CCR5) | NP_000570.1:p.Tyr3His | |
NM_001100168.2:c.7T>C (CCR5) | NP_001093638.1:p.Tyr3His | |
NM_001394783.1:c.7T>C (CCR5) MANE Select | NP_001381712.1:p.Tyr3His |