HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202377414T>A , CM000664.2:g.202377414T>A | GRCh38 |
NC_000002.11:g.203242137T>A , CM000664.1:g.203242137T>A | GRCh37 |
NC_000002.10:g.202950382T>A | NCBI36 |
NG_009363.1:g.6088T>A , LRG_712:g.6088T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.-61T>A MANE Select | ENSP00000363708.4:n.-61T>A | |
ENST00000374580.8:c.-61T>A | ENSP00000363708.4:n.-61T>A | |
NM_001204.6:c.-61T>A , LRG_712t1:c.-61T>A | NP_001195.2:n.-61T>A | |
XM_011511687.1:c.-61T>A | XP_011509989.1:n.-61T>A | |
XM_011511688.1:c.-61T>A | XP_011509990.1:n.-61T>A | |
NM_001204.7:c.-61T>A MANE Select | NP_001195.2:n.-61T>A |