HGVS | Genome Assembly |
---|---|
NC_000006.12:g.143485191A>G , CM000668.2:g.143485191A>G | GRCh38 |
NC_000006.11:g.143806328A>G , CM000668.1:g.143806328A>G | GRCh37 |
NC_000006.10:g.143848021A>G | NCBI36 |
NG_008459.1:g.39411A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367591.5:c.981A>G MANE Select | ENSP00000356563.4:p.Pro327= | |
ENST00000367591.4:c.981A>G | ENSP00000356563.4:p.Pro327= | |
ENST00000585848.1:n.120A>G | ||
NM_003630.2:c.981A>G | NP_003621.1:p.Pro327= | |
NM_003630.3:c.981A>G MANE Select | NP_003621.1:p.Pro327= |