HGVS | Genome Assembly |
---|---|
NC_000002.12:g.219060513T= , CM000664.2:g.219060513T= | GRCh38 |
NC_000002.11:g.219925235T= , CM000664.1:g.219925235T= | GRCh37 |
NC_000002.10:g.219633479T= | NCBI36 |
NG_016741.1:g.5004A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295731.7:c.-46A= MANE Select | ENSP00000295731.5:n.-46A= | |
NM_002181.3:c.-46A= | NP_002172.2:n.-46A= | |
NM_002181.4:c.-46A= MANE Select | NP_002172.2:n.-46A= |