HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31861366A= , CM000668.2:g.31861366A= | GRCh38 |
NC_000006.11:g.31829143A= , CM000668.1:g.31829143A= | GRCh37 |
NC_000006.10:g.31937122A= | NCBI36 |
NG_008201.1:g.6567T= | |
NG_023058.1:g.22681T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.437T= MANE Select | ENSP00000364782.4:p.Val146= | |
ENST00000677054.1:n.1114T= | ||
ENST00000677512.1:n.545T= | ||
ENST00000678869.1:n.545T= | ||
ENST00000375631.4:c.437T= | ENSP00000364782.4:p.Val146= | |
ENST00000480384.1:n.466T= | ||
ENST00000491768.5:c.437T= | ENSP00000433127.1:p.Val146= | |
ENST00000495807.1:n.1005T= | ||
NM_000434.3:c.437T= | NP_000425.1:p.Val146= | |
NM_000434.4:c.437T= MANE Select | NP_000425.1:p.Val146= |