HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31125718T>C , CM000668.2:g.31125718T>C | GRCh38 |
NC_000006.11:g.31093495T>C , CM000668.1:g.31093495T>C | GRCh37 |
NC_000006.10:g.31201474T>C | NCBI36 |
NG_021348.1:g.15888T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259881.10:c.-186T>C MANE Select | ENSP00000259881.9:n.-186T>C | |
ENST00000259881.9:c.-186T>C | ENSP00000259881.9:n.-186T>C | |
ENST00000479581.5:n.61+10827T>C | ||
ENST00000548049.1:n.159T>C | ||
ENST00000550838.1:n.59-21T>C | ||
ENST00000552747.1:n.53+10827T>C | ||
NM_014068.2:c.-186T>C | NP_054787.2:n.-186T>C | |
NM_014068.3:c.-186T>C MANE Select | NP_054787.2:n.-186T>C |