HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31125695T>A , CM000668.2:g.31125695T>A | GRCh38 |
NC_000006.11:g.31093472T>A , CM000668.1:g.31093472T>A | GRCh37 |
NC_000006.10:g.31201451T>A | NCBI36 |
NG_021348.1:g.15865T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259881.10:c.-209T>A MANE Select | ENSP00000259881.9:n.-209T>A | |
ENST00000259881.9:c.-209T>A | ENSP00000259881.9:n.-209T>A | |
ENST00000479581.5:n.61+10804T>A | ||
ENST00000548049.1:n.136T>A | ||
ENST00000550838.1:n.59-44T>A | ||
ENST00000552747.1:n.53+10804T>A | ||
NM_014068.2:c.-209T>A | NP_054787.2:n.-209T>A | |
NM_014068.3:c.-209T>A MANE Select | NP_054787.2:n.-209T>A |