HGVS | Genome Assembly |
---|---|
NC_000003.12:g.138945584G>A , CM000665.2:g.138945584G>A | GRCh38 |
NC_000003.11:g.138664426G>A , CM000665.1:g.138664426G>A | GRCh37 |
NC_000003.10:g.140147116G>A | NCBI36 |
NG_012454.1:g.6557C>T | |
NG_029796.1:g.3351G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648323.1:c.*8C>T MANE Select | ENSP00000497217.1:n.*8C>T | |
ENST00000330315.3:c.*8C>T | ENSP00000333188.3:n.*8C>T | |
NM_023067.3:c.*8C>T | NP_075555.1:n.*8C>T | |
NM_023067.4:c.*8C>T MANE Select | NP_075555.1:n.*8C>T |