HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31125759T= , CM000668.2:g.31125759T= | GRCh38 |
NC_000006.11:g.31093536T= , CM000668.1:g.31093536T= | GRCh37 |
NC_000006.10:g.31201515T= | NCBI36 |
NG_021348.1:g.15929T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259881.10:c.-145T= MANE Select | ENSP00000259881.9:n.-145T= | |
ENST00000259881.9:c.-145T= | ENSP00000259881.9:n.-145T= | |
ENST00000479581.5:n.61+10868T= | ||
ENST00000548049.1:n.200T= | ||
ENST00000550838.1:n.79T= | ||
ENST00000552747.1:n.53+10868T= | ||
NM_014068.2:c.-145T= | NP_054787.2:n.-145T= | |
NM_014068.3:c.-145T= MANE Select | NP_054787.2:n.-145T= |