HGVS | Genome Assembly |
---|---|
NC_000006.12:g.143485136T>A , CM000668.2:g.143485136T>A | GRCh38 |
NC_000006.11:g.143806273T>A , CM000668.1:g.143806273T>A | GRCh37 |
NC_000006.10:g.143847966T>A | NCBI36 |
NG_008459.1:g.39356T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367591.5:c.942-16T>A MANE Select | ENSP00000356563.4:n.942-16T>A | |
ENST00000367591.4:c.942-16T>A | ENSP00000356563.4:n.942-16T>A | |
ENST00000585848.1:n.65T>A | ||
NM_003630.2:c.942-16T>A | NP_003621.1:n.942-16T>A | |
NM_003630.3:c.942-16T>A MANE Select | NP_003621.1:n.942-16T>A |