HGVS | Genome Assembly |
---|---|
NC_000002.12:g.233618561T= , CM000664.2:g.233618561T= | GRCh38 |
NC_000002.11:g.234527207T= , CM000664.1:g.234527207T= | GRCh37 |
NC_000002.10:g.234191946T= | NCBI36 |
NG_002601.2:g.33818T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373450.5:c.854T= MANE Select | ENSP00000362549.4:p.Met285= | |
ENST00000373450.4:c.854T= | ENSP00000362549.4:p.Met285= | |
NM_019076.4:c.854T= | NP_061949.3:p.Met285= | |
NM_019076.5:c.854T= MANE Select | NP_061949.3:p.Met285= |