HGVS | Genome Assembly |
---|---|
NC_000013.11:g.32315478T= , CM000675.2:g.32315478T= | GRCh38 |
NC_000013.10:g.32889615T= , CM000675.1:g.32889615T= | GRCh37 |
NC_000013.9:g.31787615T= | NCBI36 |
NG_012772.3:g.4999T= , LRG_293:g.4999T= | |
NG_017006.1:g.1477A= | |
NG_017006.2:g.4886A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000544455.6:c.-40+333T= | ENSP00000439902.1:n.-40+333T= | |
ENST00000380152.7:c.-229T= | ENSP00000369497.3:n.-229T= | |
XM_011535203.1:c.-40+333T= | XP_011533505.1:n.-40+333T= | |
XM_011535204.1:c.-229T= | XP_011533506.1:n.-229T= | |
XM_011535205.1:c.-229T= | XP_011533507.1:n.-229T= |