HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31125704C= , CM000668.2:g.31125704C= | GRCh38 |
NC_000006.11:g.31093481C= , CM000668.1:g.31093481C= | GRCh37 |
NC_000006.10:g.31201460C= | NCBI36 |
NG_021348.1:g.15874C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259881.10:c.-200C= MANE Select | ENSP00000259881.9:n.-200C= | |
ENST00000259881.9:c.-200C= | ENSP00000259881.9:n.-200C= | |
ENST00000479581.5:n.61+10813C= | ||
ENST00000548049.1:n.145C= | ||
ENST00000550838.1:n.59-35C= | ||
ENST00000552747.1:n.53+10813C= | ||
NM_014068.2:c.-200C= | NP_054787.2:n.-200C= | |
NM_014068.3:c.-200C= MANE Select | NP_054787.2:n.-200C= |