HGVS | Genome Assembly |
---|---|
NC_000004.12:g.177442416A= , CM000666.2:g.177442416A= | GRCh38 |
NC_000004.11:g.178363570A= , CM000666.1:g.178363570A= | GRCh37 |
NC_000004.10:g.178600564A= | NCBI36 |
NG_011845.2:g.5088T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264595.7:c.-41T= MANE Select | ENSP00000264595.2:n.-41T= | |
ENST00000264595.6:c.-41T= | ENSP00000264595.2:n.-41T= | |
NM_000027.3:c.-41T= | NP_000018.2:n.-41T= | |
NM_001171988.1:c.-41T= | NP_001165459.1:n.-41T= | |
NR_033655.1:n.88T= | ||
XM_006714123.2:c.-41T= | XP_006714186.1:n.-41T= | |
XR_001741155.2:n.54T= | ||
NM_000027.4:c.-41T= MANE Select | NP_000018.2:n.-41T= | |
NM_001171988.2:c.-41T= | NP_001165459.1:n.-41T= | |
NR_033655.2:n.22T= |