HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160037482C>A , CM000663.2:g.160037482C>A | GRCh38 |
NC_000001.10:g.160007272C>A , CM000663.1:g.160007272C>A | GRCh37 |
NC_000001.9:g.158273896C>A | NCBI36 |
NG_016411.1:g.37690G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000509700.2:c.671+4352G>T | ||
ENST00000637644.1:c.487+4564G>T | ENSP00000490282.1:n.487+4564G>T | |
ENST00000639408.1:c.587+3020G>T | ENSP00000491635.1:n.587+3020G>T | |
ENST00000640914.1:c.224+3020G>T | ||
ENST00000644903.1:c.*3911G>T MANE Select | ENSP00000495557.1:n.*3911G>T | |
ENST00000368089.3:c.*3911G>T | ENSP00000357068.3:n.*3911G>T | |
NM_002241.4:c.*3911G>T | NP_002232.2:n.*3911G>T | |
NM_002241.5:c.*3911G>T MANE Select | NP_002232.2:n.*3911G>T |