HGVS | Genome Assembly |
---|---|
NC_000002.12:g.25161079C= , CM000664.2:g.25161079C= | GRCh38 |
NC_000002.11:g.25383948C= , CM000664.1:g.25383948C= | GRCh37 |
NC_000002.10:g.25237452C= | NCBI36 |
NG_008997.1:g.12612G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000395826.7:c.*2G= MANE Select | ENSP00000379170.2:n.*2G= | |
ENST00000264708.7:c.*2G= | ENSP00000264708.3:n.*2G= | |
ENST00000380794.5:c.*2G= | ENSP00000370171.1:n.*2G= | |
ENST00000395826.6:c.*2G= | ENSP00000379170.2:n.*2G= | |
ENST00000405623.5:c.*2G= | ENSP00000384092.1:n.*2G= | |
NM_000939.2:c.*2G= | NP_000930.1:n.*2G= | |
NM_001035256.1:c.*2G= | NP_001030333.1:n.*2G= | |
XM_011532917.1:c.*2G= | XP_011531219.1:n.*2G= | |
NM_000939.3:c.*2G= | NP_000930.1:n.*2G= | |
NM_001035256.2:c.*2G= | NP_001030333.1:n.*2G= | |
NM_001319204.1:c.*2G= | NP_001306133.1:n.*2G= | |
NM_001319205.1:c.*2G= | NP_001306134.1:n.*2G= | |
NM_000939.4:c.*2G= MANE Select | NP_000930.1:n.*2G= | |
NM_001319204.2:c.*2G= | NP_001306133.1:n.*2G= | |
NM_001319205.2:c.*2G= | NP_001306134.1:n.*2G= | |
NM_001035256.3:c.*2G= | NP_001030333.1:n.*2G= |