HGVS | Genome Assembly |
---|---|
NC_000016.10:g.68737411C= , CM000678.2:g.68737411C= | GRCh38 |
NC_000016.9:g.68771314C= , CM000678.1:g.68771314C= | GRCh37 |
NC_000016.8:g.67328815C= | NCBI36 |
NG_008021.1:g.5120C= , LRG_301:g.5120C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261769.10:c.-5C= MANE Select | ENSP00000261769.4:n.-5C= | |
ENST00000261769.9:c.-5C= | ENSP00000261769.4:n.-5C= | |
ENST00000422392.6:c.-5C= | ENSP00000414946.2:n.-5C= | |
ENST00000566510.5:c.-5C= | ENSP00000458139.1:n.-5C= | |
ENST00000566612.5:c.-5C= | ENSP00000454782.1:n.-5C= | |
ENST00000611625.4:c.-5C= | ENSP00000481063.1:n.-5C= | |
ENST00000612417.4:c.-5C= | ENSP00000478360.1:n.-5C= | |
ENST00000621016.4:c.-5C= | ENSP00000480664.1:n.-5C= | |
NM_004360.3:c.-5C= , LRG_301t1:c.-5C= | NP_004351.1:n.-5C= | |
NM_001317184.1:c.-5C= | NP_001304113.1:n.-5C= | |
NM_001317185.1:c.-1620C= | NP_001304114.1:n.-1620C= | |
NM_001317186.1:c.-1824C= | NP_001304115.1:n.-1824C= | |
NM_004360.4:c.-5C= | NP_004351.1:n.-5C= | |
NM_004360.5:c.-5C= MANE Select | NP_004351.1:n.-5C= | |
NM_001317184.2:c.-5C= | NP_001304113.1:n.-5C= | |
NM_001317185.2:c.-1620C= | NP_001304114.1:n.-1620C= | |
NM_001317186.2:c.-1824C= | NP_001304115.1:n.-1824C= |