HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442426C= , CM000666.2:g.177442426C= | GRCh38 |
NC_000004.11:g.178363580C= , CM000666.1:g.178363580C= | GRCh37 |
NC_000004.10:g.178600574C= | NCBI36 |
NG_011845.2:g.5078G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264595.7:c.-51G= MANE Select | ENSP00000264595.2:n.-51G= | |
ENST00000264595.6:c.-51G= | ENSP00000264595.2:n.-51G= | |
NM_000027.3:c.-51G= | NP_000018.2:n.-51G= | |
NM_001171988.1:c.-51G= | NP_001165459.1:n.-51G= | |
NR_033655.1:n.78G= | ||
XM_006714123.2:c.-51G= | XP_006714186.1:n.-51G= | |
XR_001741155.2:n.44G= | ||
NM_000027.4:c.-51G= MANE Select | NP_000018.2:n.-51G= | |
NM_001171988.2:c.-51G= | NP_001165459.1:n.-51G= | |
NR_033655.2:n.12G= |