HGVS | Genome Assembly |
---|---|
NC_000003.12:g.46372976T= , CM000665.2:g.46372976T= | GRCh38 |
NC_000003.11:g.46414467T= , CM000665.1:g.46414467T= | GRCh37 |
NC_000003.10:g.46389471T= | NCBI36 |
NG_012637.1:g.7835T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000292303.5:c.74T= (CCR5) MANE Select | ENSP00000292303.4:p.Val25= | |
ENST00000292303.4:c.74T= (CCR5) | ENSP00000292303.4:p.Val25= | |
ENST00000445772.1:c.74T= (CCR5) | ENSP00000404881.1:p.Val25= | |
NM_000579.3:c.74T= (CCR5) | NP_000570.1:p.Val25= | |
NM_001100168.1:c.74T= (CCR5) | NP_001093638.1:p.Val25= | |
NR_125406.1:n.392-1559A= (CCR5AS) | ||
NM_000579.4:c.74T= (CCR5) | NP_000570.1:p.Val25= | |
NM_001100168.2:c.74T= (CCR5) | NP_001093638.1:p.Val25= | |
NM_001394783.1:c.74T= (CCR5) MANE Select | NP_001381712.1:p.Val25= |