HGVS | Genome Assembly |
---|---|
NC_000023.11:g.133536117C= , CM000685.2:g.133536117C= | GRCh38 |
NC_000023.10:g.132670145C= , CM000685.1:g.132670145C= | GRCh37 |
NC_000023.9:g.132497811C= | NCBI36 |
NG_009286.1:g.454522G= , LRG_505:g.454522G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000689310.1:c.*7G= | ENSP00000510438.1:n.*7G= | |
ENST00000370818.8:c.*7G= MANE Select | ENSP00000359854.3:n.*7G= | |
ENST00000394299.7:c.*7G= | ENSP00000377836.2:n.*7G= | |
ENST00000669691.1:n.816G= | ||
ENST00000370818.7:c.*7G= | ENSP00000359854.3:n.*7G= | |
ENST00000394299.6:c.*7G= | ENSP00000377836.2:n.*7G= | |
NM_001164617.1:c.*7G= | NP_001158089.1:n.*7G= | |
NM_001164618.1:c.*7G= | NP_001158090.1:n.*7G= | |
NM_001164619.1:c.*7G= | NP_001158091.1:n.*7G= | |
NM_004484.3:c.*7G= , LRG_505t1:c.*7G= | NP_004475.1:n.*7G= | |
NM_001164617.2:c.*7G= | NP_001158089.1:n.*7G= | |
NM_001164618.2:c.*7G= | NP_001158090.1:n.*7G= | |
NM_001164619.2:c.*7G= | NP_001158091.1:n.*7G= | |
NM_004484.4:c.*7G= MANE Select | NP_004475.1:n.*7G= |