HGVS | Genome Assembly |
---|---|
NC_000010.11:g.49611743T>A , CM000672.2:g.49611743T>A | GRCh38 |
NC_000010.10:g.50819789T>A , CM000672.1:g.50819789T>A | GRCh37 |
NC_000010.9:g.50489795T>A | NCBI36 |
NG_011797.1:g.7649T>A | |
NG_053144.1:g.6443T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000374115.5:c.1003T>A (SLC18A3) MANE Select | ENSP00000363229.3:p.Phe335Ile | |
ENST00000339797.5:c.-69+2544T>A (CHAT) | ENSP00000343486.1:n.-69+2544T>A | |
ENST00000374115.4:c.1003T>A (SLC18A3) | ENSP00000363229.3:p.Phe335Ile | |
NM_003055.2:c.1003T>A (SLC18A3) | NP_003046.2:p.Phe335Ile | |
NM_020984.3:c.-69+2544T>A (CHAT) | NP_066264.3:n.-69+2544T>A | |
NM_003055.3:c.1003T>A (SLC18A3) MANE Select | NP_003046.2:p.Phe335Ile | |
NM_020984.4:c.-69+2544T>A (CHAT) | NP_066264.4:n.-69+2544T>A |